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            [name] => FSMS Fundamentals based on ISO/FSSC 22000 Training Course
            [title_name] => FSMS Fundamentals based on ISO/FSSC 22000 Training Course
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            [cat_desc] => &lt;p&gt;
	The focus of the &lt;strong&gt;FSMS Fundamentals based on FSSC 22000 Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Food Safety Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of FSSC 22000 plus the business case for adopting FSSC 22000&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the &lt;strong&gt;FSMS Fundamentals based on FSSC 22000 Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Food Safety Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of FSSC 22000 plus the business case for adopting FSSC 22000&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Our training demonstrates to the Learner the benefits of adopting the unique Kelmac Group® &lt;strong&gt;One System Model&lt;/strong&gt; for enhancing organizational compliance, effectiveness and efficiency based on utilizing Business Process Management to enhance ISO.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 1-day (8hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm&lt;/li&gt;
	&lt;li&gt;
		Ideal for those looking to get started &amp;amp; understand the requirements of Food Safety Management Systems &amp;amp; FSSC 22000.&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Business Case for FSSC 22000 and the Relationship with with Safe Food across the Food Chain*&lt;/li&gt;
						&lt;li&gt;
							Overview of GFSI Approved Schemes&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex S&lt;/li&gt;
						&lt;li&gt;
							New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							External and Internal Issues, Interested Party Requirements, Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Top Management &amp;amp; Business Processes*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;FSSC 22000 - Context of the Organization&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The New Requirements for Context of the Organization&lt;/li&gt;
						&lt;li&gt;
							The Organizations External and Internal Issues, Interested Parties, their Needs, Significance, Monitoring and Measurement&lt;/li&gt;
						&lt;li&gt;
							The PDCA Cycle and the Process-based Food Safety Management System Model for ISO/FSSC 22000&lt;/li&gt;
						&lt;li&gt;
							The Organization Business Model, Alignment with the Food Safety Management System Process Model and Benefits*&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence &amp;amp; Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;FSSC 22000 - Leadership&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;FSSC 22000 - Planning of the FSMS&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Planning of the Food Safety Management System&lt;/li&gt;
						&lt;li&gt;
							Process Terminology, Processes &amp;amp; Process Controls, Risks and Opportunities*&lt;/li&gt;
						&lt;li&gt;
							Food Safety Objectives and Plans to Achieve Them&lt;/li&gt;
						&lt;li&gt;
							Management of Change&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;FSSC 22000 - Support&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Support&lt;/li&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Awareness and Communications&lt;/li&gt;
						&lt;li&gt;
							Annex SL Requirements for Documented Information and How It Differs from Previous Management System Requirements&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;FSSC 22000 - Operation&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Operation&lt;/li&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Operational Planning and Control, specifically HACCP and Outsourcing&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;FSSC 22000 - Performance Evaluation&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Performance Evaluation*&lt;/li&gt;
						&lt;li&gt;
							The Requirements for Monitoring, Measurement, Analysis and Evaluation*&lt;/li&gt;
						&lt;li&gt;
							FSMS Verification*&lt;/li&gt;
						&lt;li&gt;
							Internal Auditing and Management Review*&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence &amp;amp; Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;FSSC 22000 - Improvement&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Improvement*&lt;/li&gt;
						&lt;li&gt;
							The Requirements for Managing Non-Conformity and Corrective Action, and Continual Improvement and updating the FSMS*&lt;/li&gt;
						&lt;li&gt;
							Certification and Accreditation*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented FSMS &lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented FSMS from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented FSMS Case Study available including an ISO/FSSC 22000 Food Safety Policy Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; Dairy – Milk Processing&amp;nbsp; HACCP System and related documented templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					One System Model&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The one system model is based on utilizing Business Process Management to enhance ISO based Management Systems.&lt;/p&gt;
				&lt;p&gt;
					Our course is unlike our competitors as we will outline a methodology for developing and implementing an Food Safety Management System based upon the requirements of FSSC 22000, where the FSMS is integrated with the organization’s business model.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Others train followers, we train leaders™&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					More Topics Covered In More Depth&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					In this course, we cover 14 topics in more depth than any of our competitors!&lt;/p&gt;
				&lt;p&gt;
					If you look at other courses, they are largely focused on knowledge based learning which does not cover all requirements of FSSC 22000.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br /&gt;

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				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
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			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
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            [name] => QMS Fundamentals based on ISO 9001:2015 Training Course
            [title_name] => QMS Fundamentals based on ISO 9001:2015 Training Course | Kelmac Group UK
            [cert_name] =>  
            [cert_name_line1] => QMS Fundamentals based on
            [cert_name_line2] => ISO 9001:2015 Training Course
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            [cat_desc] => &lt;p&gt;
	The focus of&amp;nbsp;our &lt;strong&gt;QMS Fundamentals based on ISO 9001:2015 Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Quality Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 9001:2015 plus the business case for adopting ISO 9001.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of&amp;nbsp;our &lt;strong&gt;QMS Fundamentals based on ISO 9001:2015 Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Quality Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 9001:2015 plus the business case for adopting ISO 9001.&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Our training demonstrates to the Learner the benefits of adopting the unique Kelmac Group® One System Model for enhancing organizational compliance, effectiveness and efficiency based on utilizing Business Process Management to enhance ISO.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 1-day (8hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm&lt;/li&gt;
	&lt;li&gt;
		Ideal for those looking to get started &amp;amp; understand the requirements of Quality Management Systems and ISO 9001:2015&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The Business Case for ISO 9001:2015 and the Relationship with Customer Satisfaction*&lt;/li&gt;&lt;li&gt;Purpose and Impact of Annex SL&lt;/li&gt;&lt;li&gt;New and Revised Terminology&lt;/li&gt;&lt;li&gt;The Relationship between External and Internal Issues, Interested Party Requirements, Risks and Opportunities, Top&lt;/li&gt;&lt;li&gt;Management and Business Processes*&amp;nbsp;&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;I&lt;/strong&gt;&lt;b&gt;SO 9001:2015 – Context of the Organisation&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The New Requirements for Context of the Organisation&lt;/li&gt;&lt;li&gt;The Organizations External and Internal Issues, Interested Parties, their Needs, Significance, Monitoring and Measurement&lt;/li&gt;&lt;li&gt;The PDCA Cycle and the Process-based Quality Management System Model for ISO 9001:2015&lt;/li&gt;&lt;li&gt;The Organisation Business Model*&lt;/li&gt;&lt;li&gt;Alignment with the Quality Management System Process Model [BPMS] and Benefits*&lt;/li&gt;&lt;li&gt;Audit Methods, Evidence and Sources&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;I&lt;/strong&gt;&lt;b&gt;SO 9001:2015 – Leadership&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The New and Enhanced Requirements for Leadership&lt;/li&gt;&lt;li&gt;The Seven Principles of Quality Management&lt;/li&gt;&lt;li&gt;Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;&lt;b&gt;ISO 9001:2015 – Planning of the QMS&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The Requirements for Planning of the Quality Management System&lt;/li&gt;&lt;li&gt;Process Terminology, Processes and Process Controls*&lt;/li&gt;&lt;li&gt;Risks and Opportunities*&lt;/li&gt;&lt;li&gt;Quality Objectives and Plans to achieve the Management of Change&lt;/li&gt;&lt;li&gt;Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;&lt;b&gt;ISO 9001:2015 – Support&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The Requirements for Support&lt;/li&gt;&lt;li&gt;The New and Enhanced Requirements for Awareness and Communications&lt;/li&gt;&lt;li&gt;Annex SL Requirements for Documented Information and How It Differs from Previous Management System Requirements&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;&lt;b&gt;ISO 9001:2015 – Operation&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The Requirements for Operation&lt;/li&gt;&lt;li&gt;The New and Enhanced Requirements for Operational Planning and Control, specifically Outsourcing&lt;/li&gt;&lt;li&gt;Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;&lt;b&gt;ISO 9001:2015 – Performance Evaluation&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The Requirements for Performance Evaluation*&lt;/li&gt;&lt;li&gt;The Requirements for Monitoring, Measurement, Analysis and Evaluation*&lt;/li&gt;&lt;li&gt;Internal Auditing and Management Review*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;&lt;b&gt;ISO 9001:2015 – Improvement&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;The Requirements for Improvement*&lt;/li&gt;&lt;li&gt;The Requirements for Managing Non-Conformity and Corrective Action, and Continual Improvement*&lt;/li&gt;&lt;li&gt;Certification and Accreditation*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;
            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented QMS&lt;span&gt;Why is our course the best? &lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will have access to the almost full documented QMS from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented QMS Case Study available including a ISO 9001:2015 Quality Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; and related documented templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					One System Model&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The one system model is based on utilizing Business Process Management to enhance ISO based Management Systems.&lt;/p&gt;
				&lt;p&gt;
					Our course is unlike our competitors as we will outline a methodology for developing and implementing an Quality Management System based upon the requirements of ISO 9001:2015, where the QMS is integrated with the organization’s business model.&amp;nbsp; Others train followers, we train leaders™&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					11 Topics Covered In More Depth&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					In this course, we cover 11 topics in more depth than any of our competitors.&lt;/p&gt;
				&lt;p&gt;
					If you look other courses they are largely knowledge based and focused on most but importantly they do not cover all requirements of ISO 9001:2015.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				Not All Training Is Created Equal&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/144385897&quot; webkitallowfullscreen=&quot;&quot; width=&quot;500&quot;&gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => QMS Fundamentals based on ISO 13485:2016 Training Course
            [title_name] => QMS Fundamentals based on ISO 13485:2016 Training Course | Kelmac Group UK
            [cert_name] => 
            [cert_name_line1] => QMS Fundamentals based on
            [cert_name_line2] => ISO 13485:2016 Training Course
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	The focus of the Kelmac Group®&amp;nbsp;&lt;strong&gt;QMS Fundamentals based on ISO 13485:2016&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Quality Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 13485:2016 plus the business case for adopting ISO 13485:2016&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the Kelmac Group®&amp;nbsp;&lt;strong&gt;QMS Fundamentals based on ISO 13485:2016&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Quality Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 13485:2016 plus the business case for adopting ISO 13485:2016.&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Our training demonstrates to the Learner the beneﬁts of adopting the unique Kelmac Group® One System Model for enhancing organizational compliance, effectiveness and efﬁciency based on utilizing Business Process Management to enhance ISO.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 1-day (8hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finsh Times: 08:00am - 17:30pm&lt;/li&gt;
	&lt;li&gt;
		Ideal for those looking to get started &amp;amp; understand the requirements of Quality Management Systems and ISO 13485:2016&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;div class=&quot;course-learning-title&quot;&gt;
					&lt;div class=&quot;course-learning-title&quot;&gt;
						&lt;img src=&quot;/images/accrediation.jpg&quot; /&gt;&amp;nbsp;Course Learning TopicsWhat does the course cover?&lt;br /&gt;
						&lt;ul class=&quot;clearfix&quot;&gt;
							&lt;li class=&quot;learning_topic&quot;&gt;
								&lt;p&gt;
									&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
								&lt;ul&gt;
									&lt;li&gt;
										The Business Case for ISO 13485 :2016 and the Relationship with Product Safety and Effectiveness&lt;/li&gt;
									&lt;li&gt;
										Key ISO 13485:2016 Terms*&lt;/li&gt;
									&lt;li&gt;
										The Relationship with the Medical Device Life Cycle and Regulatory Framework*&lt;/li&gt;
									&lt;li&gt;
										The Family of Medical Device Standards including Software*&lt;/li&gt;
									&lt;li&gt;
										Overview of various Medical Device Statutory and Regulatory Requirements*&lt;/li&gt;
								&lt;/ul&gt;
								&lt;p&gt;
									&lt;strong&gt;ISO 13485 – General Requirements for a Quality Management System&lt;/strong&gt;&lt;/p&gt;
								&lt;ul&gt;
									&lt;li&gt;
										The Scope of the QMS&lt;/li&gt;
									&lt;li&gt;
										The PDCA Cycle and the Process-based Quality Management System Model for ISO 13485:2016*&lt;/li&gt;
									&lt;li&gt;
										The Organization Business Model, Alignment with the Medical Device Product Life Cycle and Beneﬁts*&lt;/li&gt;
									&lt;li&gt;
										Medical Device Documented QMS Requirements&lt;/li&gt;
									&lt;li&gt;
										Audit Evidence and Sources*&lt;/li&gt;
								&lt;/ul&gt;
							&lt;/li&gt;
							&lt;li class=&quot;learning_topic&quot;&gt;
								&lt;p&gt;
									&lt;strong&gt;ISO 13485 - Management Responsibility&lt;/strong&gt;&lt;/p&gt;
							&lt;/li&gt;
							&lt;li class=&quot;learning_topic&quot;&gt;
								&lt;ul&gt;
									&lt;li&gt;
										The New and Enhanced Requirements for Leadership&lt;/li&gt;
									&lt;li&gt;
										The Seven Principles of Quality Management Quality Policy&lt;/li&gt;
									&lt;li&gt;
										Quality Objectives and Plans to Achieve Them&lt;/li&gt;
									&lt;li&gt;
										Management of Change Responsibility&lt;/li&gt;
									&lt;li&gt;
										Authority and Communication&lt;/li&gt;
									&lt;li&gt;
										Management Review&lt;/li&gt;
									&lt;li&gt;
										Audit Evidence and Sources*&lt;/li&gt;
								&lt;/ul&gt;
							&lt;/li&gt;
							&lt;li class=&quot;learning_topic&quot;&gt;
								&lt;p&gt;
									&lt;strong&gt;ISO 13485 – Resources&lt;/strong&gt;&lt;/p&gt;
								&lt;ul&gt;
									&lt;li&gt;
										The Requirements for Resources to Support the Development, Implementation and Maintenance of the Medical Device &amp;nbsp;Quality Management System&lt;/li&gt;
									&lt;li&gt;
										Human Resources, Infra-structure and Work Environment&lt;/li&gt;
									&lt;li&gt;
										Audit Evidence and Sources*&amp;nbsp;&lt;/li&gt;
								&lt;/ul&gt;
								&lt;p&gt;
									&lt;strong&gt;ISO 13485 – Product Realization&lt;/strong&gt;&lt;/p&gt;
								&lt;ul&gt;
									&lt;li&gt;
										The Requirements for the Medical Device Life Cycle&lt;/li&gt;
									&lt;li&gt;
										Planning including Risk Management [ISO 14971]&lt;/li&gt;
									&lt;li&gt;
										Customer Requirements&lt;/li&gt;
									&lt;li&gt;
										Design Controls, Purchasing, Production, Installation &amp;amp; Servicing&lt;/li&gt;
									&lt;li&gt;
										Monitoring and Measuring Devices&lt;/li&gt;
								&lt;/ul&gt;
								&lt;p&gt;
									&lt;strong&gt;ISO 13485 – Measurement, Analysis and Improvement&lt;/strong&gt;&lt;/p&gt;
								&lt;ul&gt;
									&lt;li&gt;
										The requirements for Monitoring and Measurement&lt;/li&gt;
									&lt;li&gt;
										Control of Non-Conforming Product&lt;/li&gt;
									&lt;li&gt;
										Analysis of Data and Improvement&lt;/li&gt;
									&lt;li&gt;
										Audit Evidence and Sources*&lt;/li&gt;
									&lt;li&gt;
										Certiﬁcation and Accreditation*&lt;/li&gt;
								&lt;/ul&gt;
							&lt;/li&gt;
							&lt;li&gt;
								&amp;nbsp;&lt;/li&gt;
						&lt;/ul&gt;
					&lt;/div&gt;
					&lt;div class=&quot;course_certification_terms&quot;&gt;
						&lt;p&gt;
							&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br /&gt;
							&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
					&lt;/div&gt;
					&lt;div class=&quot;course_certification&quot;&gt;
						&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot; /&gt;
						&lt;h4&gt;
							Course Certification&lt;/h4&gt;
						&lt;div class=&quot;course_certification_description&quot;&gt;
							&lt;p&gt;
								This course is certified by Kelmac Group.&lt;/p&gt;
						&lt;/div&gt;
					&lt;/div&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br /&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Assessment of Process Effectiveness&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented QMS [Medical Devices] from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional ﬁnancial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&lt;br /&gt;
					&amp;nbsp;&lt;br /&gt;
					We boast the most comprehensive documented QMS [MD] Case Study available including a ISO 13485 Quality Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; the organization’s statutory and regulatory and other legal obligations register, and the organization’s risk register, and related documented Quality templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Wider Coverage of Audit Methods&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;div&gt;
					In this course, we cover 9 topics in more depth than any of our competitors.&amp;nbsp;&lt;br /&gt;
					&amp;nbsp;&lt;/div&gt;
				&lt;div&gt;
					If you look at other courses, they are largely focused on knowledge based learning which does not cover all requirements of ISO 13485.:2016.&lt;/div&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br /&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => ISO 14001:2015 Requirements &amp; Fundamentals Training Course
            [title_name] => ISO 14001:2015 Requirements &amp; Fundamentals Training Course | Kelmac Group UK
            [cert_name] => ISO 14001:2015 Requirements &amp; Fundamentals Training Course
            [cert_name_line1] => 
            [cert_name_line2] => 
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	This is a Kelmac Group® course on the Fundamentals &amp;amp; Requirements of ISO 14001:2015, focused on facilitating the Learner understand the ISO 14001:2015 requirements and its intended outcomes. During this process, the learner will also learn to manage audit evidence and sources to fulfil the requirements of this International Environmental Management System Standard.&lt;/p&gt;

            [description] => &lt;p&gt;
	This is a Kelmac Group® course on the Fundamentals &amp;amp; Requirements of ISO 14001:2015, focused on facilitating the Learner understand the ISO 14001:2015 requirements and its intended outcomes. During this process, the learner will also learn to manage audit evidence and sources to fulfil the requirements of this International Environmental Management System Standard.&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Our training demonstrates to the Learner the benefits of adopting the unique Kelmac Group® One System Model for enhancing organizational compliance, effectiveness and efficiency based on utilizing Business Process Management to enhance ISO.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 1-day (8hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day)&lt;/li&gt;
	&lt;li&gt;
		Ideal for those looking to get started &amp;amp; understand the requirements of Environmental Management Systems and ISO 14001:2015.&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Business/Societal Case for ISO 14001:2015 and the Relationship with Environmental Performance, Protection of the Environment, and Prevention of Pollution*&lt;/li&gt;
						&lt;li&gt;
							Overview of ISO 14001 Environmental Family of Standards&lt;/li&gt;
						&lt;li&gt;
							How to Integrate with the Organization’s Business Model*&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex SL&lt;/li&gt;
						&lt;li&gt;
							New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							External and Internal Issues, Interested Party Requirements, Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Leadership&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Context of the Organization&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The New Requirements for Context of the Organization&lt;/li&gt;
						&lt;li&gt;
							The Organizations External and Internal Issues, Interested Parties, their Needs, Significance, Monitoring and Measurement&lt;/li&gt;
						&lt;li&gt;
							The PDCA Cycle and the Process-based Environmental Management System Model for ISO 14001:2015&lt;/li&gt;
						&lt;li&gt;
							Life Cycle Thinking&lt;/li&gt;
						&lt;li&gt;
							Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Leadership&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Planning of the EMS&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Planning of the Environmental Management System&lt;/li&gt;
						&lt;li&gt;
							Risks and Opportunities*&lt;/li&gt;
						&lt;li&gt;
							Environmental Objectives and Plans to achieve them including the Relationship with the Environmental Policy &amp;amp; Management Review*&lt;/li&gt;
						&lt;li&gt;
							Management of Change*&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Support&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Support&lt;/li&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Awareness and Communications&lt;/li&gt;
						&lt;li&gt;
							Annex SL Requirements for Documented Information and How It Differs from Previous Management System Requirements&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Operation&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Operation&lt;/li&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Operational Planning and Control, specifically Outsourcing&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Performance Evaluation&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Environmental Performance Evaluation*&lt;/li&gt;
						&lt;li&gt;
							The Requirements for Monitoring, Measurement, Analysis and Evaluation*&lt;/li&gt;
						&lt;li&gt;
							Internal Auditing and Management Review*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Improvement&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Improvement*&lt;/li&gt;
						&lt;li&gt;
							The Requirements for Managing Non-Conformity and Corrective Action, and Continual Improvement*&lt;/li&gt;
						&lt;li&gt;
							Certification and Accreditation*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented EMS &lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will have access to the almost full documented EMS from the &lt;strong&gt;unique Kelmac Group® assurance perspective.&lt;/strong&gt; The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at &lt;strong&gt;improving performance of the organization.&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented EMS Case Study available including an Integrated EHS (ISO 14001 &amp;amp; OHSAS 18001/ISO 45001) Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; the organization’s environmental aspects/impacts register, the organization’s statutory and regulatory and other legal obligations register, the organization’s emergency preparedness and response plan and the organization’s risk register, and related documented environmental templates and records.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					One System Model&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The one system model is based on &lt;strong&gt;utilizing Business Process Management to enhance ISO based Management Systems.&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					Our course is unlike our competitors as we will outline a methodology for developing and implementing an Environmental Management System based upon the requirements of ISO 14001:2015, where the EMS is integrated with the organization’s business model.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					&lt;strong&gt;Others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					More Topics Covered In More Depth&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					In this course, &lt;strong&gt;we cover 13 topics in more depth than any of our competitors!&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					If you look at other courses, they are largely focused on knowledge based learning which does not cover all requirements of ISO 14001.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
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            [name] => ISMS Fundamentals based on ISO/IEC 27001:2013 Training Course
            [title_name] => ISMS Fundamentals based on ISO/IEC 27001:2013 Training Course | UK
            [cert_name] => ISO/IEC 27001:2013 Core Requirements Foundation Course
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            [cat_desc] => &lt;p&gt;
	The focus of the&amp;nbsp;&lt;strong&gt;ISO 27001 Fundamentals Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Information Security Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 27001 plus the business case for adopting ISO 27001.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the&amp;nbsp;&lt;strong&gt;ISO 27001 Fundamentals Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Information Security Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 27001 plus the business case for adopting ISO 27001.&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Our training demonstrates to the Learner the benefits of adopting the unique Kelmac Group® &lt;strong&gt;One System Model&lt;/strong&gt; for enhancing organizational compliance, effectiveness and efficiency based on utilizing Business Process Management to enhance ISO.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 1-day (8hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm&lt;/li&gt;
	&lt;li&gt;
		Ideal for those looking to get started &amp;amp; understand the requirements of Information Security Management Systems &amp;amp; ISO/IEC 27001:2013.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Business Case for ISO/IEC 27001:2013 and the Relationship with Confidentiality, Integrity and Availability of the Organization’s Assets*&lt;/li&gt;
						&lt;li&gt;
							Overview of ISO 27000 Family of Standards&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex SL&lt;/li&gt;
						&lt;li&gt;
							New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							External and Internal Issues, Interested Party Requirements, Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Top Management &amp;amp; Business Processes*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO/IEC 27001 - Context of the Organization&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The New Requirements for Context of the Organization&lt;/li&gt;
						&lt;li&gt;
							The Organizations External and Internal Issues, Interested Parties, their Needs, Significance, Monitoring and Measurement&lt;/li&gt;
						&lt;li&gt;
							The PDCA Cycle and the Process-based Information Security Management System Model for ISO/IEC 27001:2013&lt;/li&gt;
						&lt;li&gt;
							The Organization Business Model, Alignment with the Information Security Management System Process Model and Benefits*&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence &amp;amp; Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO/IEC 27001 - Leadership&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Leadership&lt;/li&gt;
						&lt;li&gt;
							The ISACA&lt;/li&gt;
						&lt;li&gt;
							The Information Security Forum (ISF) and (ISC)² Twelve Principles of Information Security*&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO/IEC 27001 - Planning of the ISMS&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Planning of the Information Security Management System&lt;/li&gt;
						&lt;li&gt;
							Process Terminology, Processes &amp;amp; Process Controls, Risks and Opportunities*&lt;/li&gt;
						&lt;li&gt;
							Objectives and Plans to Achieve Them&lt;/li&gt;
						&lt;li&gt;
							Management of Change&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO/IEC 27001 - Support&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Support&lt;/li&gt;
						&lt;li&gt;
							Awareness and Communications&lt;/li&gt;
						&lt;li&gt;
							Annex SL Requirements for Documented Information and How It Differs from Previous Management System Requirements&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO/IEC 27001 - Operation&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Operation&lt;/li&gt;
						&lt;li&gt;
							The New and Enhanced Requirements for Operational Planning and Control, specifically Outsourcing&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO/IEC 27001 - Performance Evaluation*&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Performance Evaluation*&lt;/li&gt;
						&lt;li&gt;
							The Requirements for Monitoring, Measurement, Analysis and Evaluation*&lt;/li&gt;
						&lt;li&gt;
							Internal Auditing and Management Review*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO/IEC 27001 - Improvement*&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Improvement*&lt;/li&gt;
						&lt;li&gt;
							The Requirements for Managing Non-Conformity and Corrective Action, and Continual Improvement*&lt;/li&gt;
						&lt;li&gt;
							Certification and Accreditation*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? &lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented ISMS &lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented ISMS from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented ISMS Case Study available including an ISO 27001:2013 Policy Manual; Statement of Applicability; Asset/Risk Register and Risk Treatment Plan, 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; the organization’s statutory and regulatory and other legal obligations register, and the organization’s risk register, and related documented Information Security templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					One System Model&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The one system model is based on utilizing Business Process Management to enhance ISO based Management Systems.&lt;/p&gt;
				&lt;p&gt;
					Our course is unlike our competitors as we will outline a methodology for developing and implementing an Information Security Management System based upon the requirements of ISO/IEC 27001:2013, where the ISMS is integrated with the organization’s business model.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Others train followers, we train leaders™&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					More Topics Covered In More Depth&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					In this course, we cover 14 topics in more depth than any of our competitors!&lt;/p&gt;
				&lt;p&gt;
					If you look at other courses, they are largely focused on knowledge based learning which does not cover all requirements of ISO 27001.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
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			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
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	The focus of&amp;nbsp;our &lt;b&gt;CQI &amp;amp; IRCA Certified Online&amp;nbsp;&lt;/b&gt;&lt;strong&gt;ISO 9001:2015 Fundamentals Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Quality Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 9001:2015 plus the business case for adopting ISO 9001. It can be completed&lt;b&gt; anytime, anywhere -&lt;/b&gt; fully online or on the go!&lt;/p&gt;&lt;p&gt;&lt;b&gt;FREE Demo Available! &lt;/b&gt;Try our course for free!&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot;&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of&amp;nbsp;our &lt;b&gt;Online&lt;/b&gt;&lt;strong&gt;&amp;nbsp;ISO 9001:2015 Fundamentals Training Course&lt;/strong&gt;&amp;nbsp;is to comprehensively introduce Learners to Quality Management Systems and provide them with a highly insightful introduction to the purpose, intent and requirements of ISO 9001:2015 plus the business case for adopting ISO 9001. It can be completed &lt;b&gt;anytime, anywhere -&lt;/b&gt; fully online 24/7!&lt;/p&gt;&lt;p&gt;&lt;b&gt;FREE Demo Available! &lt;/b&gt;Try our course for free!&lt;b&gt;&lt;br&gt;&lt;/b&gt;&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;
	&lt;h4&gt;
		&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot;&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
	&lt;p&gt;
		This training course is a first-of-its-kind, introducing a highly interactive and yet fully online training course for those looking to gain a comprehensive &amp;amp; practical understanding of ISO 9001:2015. &lt;b&gt;We are the first provider in Ireland to launch eLearning for Quality Management &amp;amp; ISO 9001:2015 &amp;amp; now the first and only training provider in the world with a fully online CQI &amp;amp; IRCA Certified online ISO 9001:2015 Foundation Course.&lt;/b&gt;&lt;/p&gt;
&lt;/div&gt;
&lt;div class=&quot;six-step&quot;&gt;
	&lt;h4&gt;
		&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot;&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
	&lt;ul&gt;
		&lt;li&gt;
			This is a fully online training course&lt;/li&gt;&lt;li&gt;This course covers EACH clause of ISO 9001:2015&lt;/li&gt;&lt;li&gt;It is the most comprehensive course available&amp;nbsp;&lt;strong&gt;including 10 Learning Hours&lt;/strong&gt;&lt;/li&gt;
		&lt;li&gt;
			Complete anytime, anywhere&lt;/li&gt;
		&lt;li&gt;
			Ideal for those looking to get started &amp;amp; understand the requirements of Quality Management Systems and ISO 9001:2015&lt;/li&gt;&lt;li&gt;Fully Certified by CQI &amp;amp; IRCA!&lt;/li&gt;&lt;li&gt;&lt;b&gt;FREE Demo Available! &lt;/b&gt;Try our course for free!&lt;br&gt;&lt;/li&gt;
	&lt;/ul&gt;
&lt;/div&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
  &lt;div class=&quot;container clearfix&quot;&gt;
    &lt;div class=&quot;course-learning clearfix&quot;&gt;
      &lt;div class=&quot;course-learning-title&quot;&gt;
        &lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;
      &lt;/div&gt;
      &lt;ul class=&quot;clearfix&quot;&gt;
	  &lt;li class=&quot;learning_topic&quot;&gt;
		&lt;p&gt;
		  &lt;strong&gt;Module 1 - Course Introduction&lt;/strong&gt;
		&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Course Description &amp;amp; Objectives&lt;/li&gt;
		  &lt;li&gt;Course Content Overview&lt;/li&gt;
		  &lt;li&gt;Explaining the Module Structure&lt;/li&gt;
		  &lt;li&gt;Explaining the Assessment Methodology&lt;/li&gt;
		  &lt;li&gt;Certification&lt;/li&gt;
		&lt;/ul&gt;
		&lt;p&gt;&lt;b&gt;Module 2 - Introduction to QMS&lt;/b&gt;&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Purposes of a QMS&lt;/li&gt;
		  &lt;li&gt;Benefits of a QMS&lt;/li&gt;
		  &lt;li&gt;ISO 9000 Family of Standards&lt;/li&gt;
		  &lt;li&gt;Scope of ISO 9001&lt;/li&gt;
		  &lt;li&gt;Structure of ISO 9001&lt;/li&gt;
		  &lt;li&gt;Terms &amp;amp; Definitions&lt;/li&gt;
		  &lt;li&gt;Transition Challenges&lt;/li&gt;
		&lt;/ul&gt;
		&lt;p&gt;&lt;b&gt;Module 3 - Key Concepts of ISO 9001:2015&lt;/b&gt;&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Alignment with Strategic Direction&lt;/li&gt;
		  &lt;li&gt;Risk-Based Thinking&lt;/li&gt;
		  &lt;li&gt;Process Approach&lt;/li&gt;
		  &lt;li&gt;Documented Information&lt;/li&gt;
		  &lt;li&gt;Improvement, Innovation &amp;amp; Competitiveness&lt;/li&gt;
		&lt;/ul&gt;
		&lt;p&gt;&lt;b&gt;Module 4 - Principles of Quality Management&lt;/b&gt;&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Quality Management Principles&lt;/li&gt;
		  &lt;li&gt;Customer Focus&lt;/li&gt;
		  &lt;li&gt;Leadership&lt;/li&gt;
		  &lt;li&gt;People Engagement&lt;/li&gt;
		  &lt;li&gt;Process Approach&lt;/li&gt;
		  &lt;li&gt;Improvement&lt;/li&gt;
		  &lt;li&gt;Evidence-Based Decision Making&lt;/li&gt;
		  &lt;li&gt;Relationship Management&lt;/li&gt;
		&lt;/ul&gt;
	  &lt;/li&gt;
	  &lt;li class=&quot;learning_topic&quot;&gt;
		&lt;p&gt;&lt;b&gt;Module 5 - Context of the Organization&lt;/b&gt;&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Context of the Organization&lt;/li&gt;
		  &lt;li&gt;Interested Parties Requirements&lt;/li&gt;
		  &lt;li&gt;Scope of the QMS&lt;/li&gt;
		  &lt;li&gt;QMS and its Processes&lt;/li&gt;
		&lt;/ul&gt;
		&lt;p&gt;&lt;b&gt;Module 6 - Leadership &amp;amp; Planning&lt;/b&gt;&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Leadership and Commitment&lt;/li&gt;
		  &lt;li&gt;Quality Policy&lt;/li&gt;
		&lt;/ul&gt;
		&lt;p&gt;&lt;b&gt;Module 7 - Support&lt;/b&gt;&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Resources&lt;/li&gt;
		  &lt;li&gt;Competence&lt;/li&gt;
		  &lt;li&gt;Awareness&lt;/li&gt;
		  &lt;li&gt;Communication&lt;/li&gt;
		  &lt;li&gt;Documented Information&lt;/li&gt;
		&lt;/ul&gt;
		&lt;p&gt;&lt;b&gt;Module 8 - Operations&lt;/b&gt;&lt;/p&gt;
		&lt;ul&gt;
		  &lt;li&gt;Clauses 8.1, 8.2, 8.3 &amp;amp; 8.4&lt;/li&gt;
		  &lt;li&gt;Clause 8.5&lt;/li&gt;
		  &lt;li&gt;Clauses 8.6 &amp;amp; 8.7&lt;/li&gt;
		&lt;/ul&gt;
	  &lt;/li&gt;
	  &lt;li class=&quot;learning_topic&quot;&gt;
		&lt;p&gt;&lt;b&gt;Module 9 - Performance and Improvement&lt;/b&gt;&lt;/p&gt;
		&lt;ul style=&quot;margin-bottom: 0px;&quot;&gt;
		  &lt;li&gt;Monitoring, Measurement, Analysis &amp;amp; Evaluation&lt;/li&gt;
		  &lt;li&gt;Internal Audit Requirements&lt;/li&gt;
		  &lt;li&gt;Management Review Requirements&lt;/li&gt;
		  &lt;li&gt;Improvement Requirements&lt;/li&gt;
		&lt;/ul&gt;
		&lt;p&gt;&lt;b&gt;Module 10 - Final Assessment&lt;/b&gt;&lt;/p&gt;
		&lt;ul style=&quot;margin-bottom: 0px;&quot;&gt;
		  &lt;li&gt;Comprehensive 50 MCQ Test&lt;/li&gt;
		&lt;/ul&gt;
	  &lt;/li&gt;
	&lt;/ul&gt;
      &lt;div class=&quot;course_certification&quot;&gt;
        &lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
        &lt;h4&gt;
          Course Certification - CQI &amp;amp; IRCA&lt;/h4&gt;
        &lt;div class=&quot;course_certification_description&quot;&gt;
          &lt;p&gt;
            This course is fully certified by CQI/IRCA. Course ID: 1912.&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/cqi and irca course.png&quot; style=&quot;width: 250px;&quot;&gt;
          &lt;/p&gt;
        &lt;/div&gt;
      &lt;/div&gt;
    &lt;/div&gt;
  &lt;/div&gt;
&lt;/div&gt;

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			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot;&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;Learning Anytime, Anywhere&lt;/h4&gt;
				&lt;p&gt;Compared to traditional classroom training, online training offers each Learner the flexibility they crave. It no longer requires you to travel, leave home or work to attend training. You decide your own schedule and complete at your own pace. The training is available to work with your computer, mobile or tablet (internet required).&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;Highly Interactive &amp;amp; Practical&lt;/h4&gt;
				&lt;p&gt;In deciding to develop and invest in eLearning, we wanted to make sure our training was as interactive as possible within an online environment - plus ensuring our online modules contained a practical element to the study, as well as application. We have built our reputation on highly interactive, accelerated learning in the classroom and we wanted to try and bring as much of that as possible to the online environment. Others train followers, we train leaders™&lt;br&gt;&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;Variety in Learning&lt;/h4&gt;
				&lt;p&gt;In this course, with 10 learning hours, we wanted to ensure we offered a variety in methods to appeal to different learning styles. We have a mixture of interactive content, additional reading materials, with interactive assessments, scenarios and a comprehensive final assessment.&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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			&lt;h1 class=&quot;heading&quot;&gt;&lt;br&gt;&lt;/h1&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => Internal FSMS Auditor based on ISO/FSSC 22000 Training Course
            [title_name] => Internal FSMS Auditor based on ISO/FSSC 22000 Training Course | Food Safety
            [cert_name] => 
            [cert_name_line1] => Internal FSMS Auditor based on
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            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	The focus of our &lt;strong&gt;FSSC 22000 Internal Auditor&amp;nbsp;Training Course&lt;/strong&gt; is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of an FSMS based on FSSC 22000 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an FSMS, covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviors.&lt;br /&gt;
	*ISO 22000:2005&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of our &lt;strong&gt;FSSC 22000 Internal Auditor&amp;nbsp;Training Course&lt;/strong&gt; is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of an FSMS based on FSSC 22000 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an FSMS, covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviors.&lt;br /&gt;
	*ISO 22000:2005&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Provide Internal Auditors with both the confidence and ability to apply the audit assurance tools and techniques, methodology and desired behaviors to assess the organization’s FSMS processes and process controls to consistently deliver safe food across the food chain, meeting interested party and applicable statutory and regulatory requirements.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 2-day (16hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day)&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO/FSSC 22000 Requirements or have received ISO/FSSC 22000 Fundamentals training in advance of attending this course.&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

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	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Introduction to Internal Auditing&lt;/li&gt;
						&lt;li&gt;
							The role of Internal Audits and the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology and Principles&lt;/li&gt;
						&lt;li&gt;
							Audit Types and Objectives&lt;/li&gt;
						&lt;li&gt;
							Understanding the PDCA Cycle and Process Approach and their significance for Internal Auditors**&lt;/li&gt;
						&lt;li&gt;
							Internal Auditor Competence, Roles &amp;amp; Responsibilities&lt;/li&gt;
						&lt;li&gt;
							Behaviours &amp;amp; Performance Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Business Process Management**&lt;/li&gt;
						&lt;li&gt;
							Audit Planning (Process &amp;amp; Risk-based)**&lt;/li&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the on-site activities**&lt;/li&gt;
						&lt;li&gt;
							Developing an Audit Plan/Scope Audit Protocol (Checklist/Process Documentation)**&lt;/li&gt;
						&lt;li&gt;
							On-Site Audit Activities (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Opening Meeting (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Evidence, Methods &amp;amp; Procedure for Gathering Evidence (Wider Audit Methods)**&lt;/li&gt;
						&lt;li&gt;
							Interviewing and Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Handling and Managing Difficult Situations&lt;/li&gt;
						&lt;li&gt;
							Auditing Reporting (In more depth)**&lt;/li&gt;
						&lt;li&gt;
							Audit Findings, Terminology, Classification and Elements&lt;/li&gt;
						&lt;li&gt;
							Writing Audit Findings &amp;amp; the Audit Report&lt;/li&gt;
						&lt;li&gt;
							Completing the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up Strategies (In-depth)**&lt;/li&gt;
						&lt;li&gt;
							Corrective and Preventative Action including Audit Finding Closure (Robust Evaluation)**&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting (Real Life Scenario)**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
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			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Assessment of Process Effectiveness&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					To have a high performing FSMS that directly and indirectly impacts business performance requires a FSMS that is integrated with the organizations business processes.&lt;/p&gt;
				&lt;p&gt;
					Our course focuses on providing Learners with skills to provide real value and underpin Process Owner and other Stakeholder confidence – this leads to better improvements, more insightful audits, better quality information and therefore, better informed decisions.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Wider Coverage of Audit Methods&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					What sets the Kelmac Group® course apart from both the IRCA course specification and competitor courses is we develop the Learner’s competency using a wide variety of audit methods, namely interview, document review and analysis of process and product data and information and operational records.&lt;/p&gt;
				&lt;p&gt;
					By comparison, competitor courses only focus on one audit method, interview and this does not expose the FSMS Auditor to the real-life audit situation – the Kelmac Group course does.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
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            [name] => ISO 13485:2016 Internal Auditor Training Course
            [title_name] => ISO 13485:2016 Internal Auditor Training Course | Medical Devices
            [cert_name] => 
            [cert_name_line1] => Internal QMS Auditor based on
            [cert_name_line2] => ISO 13485:2016 Training Course
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	The focus of the Kelmac Group® ISO 13485:2016 Internal Auditor Classroom Learning Course is on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a product, process or department/function of a QMS based on ISO 13485:2016 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process, a product or a department/function within a QMS, covering the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviors.&lt;/p&gt;
&lt;p&gt;
	We provide Internal Auditors with both the confidence and ability to apply the audit assurance tools and techniques, methodology and desired behaviors to assess the organization’s QMS Medical Device processes and process controls to consistently provide safe &amp;amp; effective medical device products and services that meet customer and applicable statutory and regulatory requirements.&lt;/p&gt;
&lt;p&gt;
	This course is one of our most popular for training Quality Internal Auditors and is also available for onsite delivery.&lt;/p&gt;
&lt;p&gt;
	We run this training publicly in Ireland in Limerick. Just give us a call or drop us an email for more information. Our brochure for this course and all our offerings can be downloaded directly from our website via this page (see below).&lt;/p&gt;
&lt;p&gt;
	&lt;br /&gt;
	&amp;nbsp;&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the Kelmac Group® ISO 13485:2016 Internal Auditor Classroom Learning Course is on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a product, process or department/function of a QMS based on ISO 13485:2016 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process, a product or a department/function within a QMS, covering the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviors.&lt;/p&gt;
&lt;p&gt;
	We provide Internal Auditors with both the confidence and ability to apply the audit assurance tools and techniques, methodology and desired behaviors to assess the organization’s QMS Medical Device processes and process controls to consistently provide safe &amp;amp; effective medical device products and services that meet customer and applicable statutory and regulatory requirements.&lt;/p&gt;
&lt;p&gt;
	This course is one of our most popular for training Quality Internal Auditors and is also available for onsite delivery.&lt;/p&gt;
&lt;p&gt;
	We run this training publicly in Ireland in Limerick. Just give us a call or drop us an email for more information. Our brochure for this course and all our offerings can be downloaded directly from our website via this page (see below).&lt;/p&gt;
&lt;p&gt;
	&lt;br /&gt;
	&amp;nbsp;&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	We focus on consistent interpretation &amp;amp; application the requirements of ISO 14001:2015 and the ability to plan, conduct, report and follow up an audit of a&lt;br /&gt;
	different Environmental Management System scenarios to provide Assurance the Environmental Management System meets the needs of the interested parties.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 5-day (45hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 18:00pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO 14001:2015 Requirements or have completed a recognised EMS Fundamentals course based on ISO 14001:2015 prior to registering for this course.&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Introduction to Internal Auditing&lt;/li&gt;
						&lt;li&gt;
							The role of Internal Audits and the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology and Principles&lt;/li&gt;
						&lt;li&gt;
							Audit Types and Objectives&lt;/li&gt;
						&lt;li&gt;
							Understanding the PDCA Cycle and Process Approach and their significance for Internal Auditors**&lt;/li&gt;
						&lt;li&gt;
							Internal Auditor Competence, Roles &amp;amp; Responsibilities&lt;/li&gt;
						&lt;li&gt;
							Behaviors &amp;amp; Performance Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Business Process Management**&lt;/li&gt;
						&lt;li&gt;
							Audit Planning (Process &amp;amp; Risk-based)**&lt;/li&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the on-site activities**&lt;/li&gt;
						&lt;li&gt;
							Developing an Audit Plan/Scope Audit Protocol (Checklist/Process Documentation)**&lt;/li&gt;
						&lt;li&gt;
							Audit Protocol (Checklist/Process Documentation)**&lt;/li&gt;
						&lt;li&gt;
							Opening Meeting (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Evidence, Methods &amp;amp; Procedure for Gathering Evidence (Wider Audit Methods)**&lt;/li&gt;
						&lt;li&gt;
							Interviewing and Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Auditing Reporting (In more depth)**&lt;/li&gt;
						&lt;li&gt;
							Audit Findings, Terminology, Classification and Elements&lt;/li&gt;
						&lt;li&gt;
							Writing Audit Findings &amp;amp; the Audit Report&lt;/li&gt;
						&lt;li&gt;
							Completing the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up Strategies (In-depth)**&lt;/li&gt;
						&lt;li&gt;
							Corrective and Preventative Action including Audit Finding Closure (Robust Evaluation)**&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting (Real Life Scenario)**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;
	&amp;nbsp;&lt;p&gt;&lt;/p&gt;

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	&lt;div class=&quot;container clearfix&quot;&gt;
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			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
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            [name] => ISO 9001:2015 Internal Auditor Training Course | IRCA Certified
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            [cat_desc] => &lt;p&gt;
	The focus of the Kelmac Group®&lt;strong&gt; ISO 9001:2015 Internal Auditor Training Course&lt;/strong&gt; is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of a QMS based on ISO 9001:2015 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an QMS, covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviors.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the Kelmac Group®&lt;strong&gt; ISO 9001:2015 Internal Auditor Training Course&lt;/strong&gt; is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of a QMS based on ISO 9001:2015 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an QMS, covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviors.&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Provide Internal Auditors with both the confidence and ability to apply the audit assurance tools and techniques, methodology and desired behaviors to assess the organization’s QMS processes and process controls to consistently provide &lt;strong&gt;products and services that meet customer and applicable statutory and regulatory requirements and to facilitate opportunities to enhance customer satisfaction.&lt;/strong&gt;&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 2-day (16hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day)&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO 9001:2015 Requirements or have received ISO 9001:2015 Fundamentals training in advance of attending this course (IRCA Pre-requisite).&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;ul&gt;&lt;li&gt;Introduction to Internal Auditing &amp;nbsp;&lt;/li&gt;&lt;li&gt;The role of Internal Audits and the Audit Life Cycle&lt;/li&gt;&lt;li&gt;Audit Terminology and Principles&lt;/li&gt;&lt;li&gt;Audit Types and Objectives&lt;/li&gt;&lt;li&gt;Understanding the PDCA Cycle and Process Approach and their significance for Internal Auditors**&lt;/li&gt;&lt;li&gt;Horizontal &amp;amp; Vertical Auditing&lt;/li&gt;&lt;li&gt;Internal Auditor Competence, Roles &amp;amp; Responsibilities&lt;/li&gt;&lt;li&gt;Desired Behaviours &amp;amp; Performance Evaluation**&lt;/li&gt;&lt;li&gt;Audit Planning (Process &amp;amp; Risk-based)**&lt;/li&gt;&lt;li&gt;Initiating &amp;amp; Preparing for the on-site activities**&lt;/li&gt;&lt;li&gt;Developing an Audit Plan/Scope Audit Protocol (Checklist/Documentation)**&lt;/li&gt;&lt;li&gt;On-Site Audit Activities (Real Life Scenario)**&lt;/li&gt;&lt;li&gt;Opening Meeting Evidence, Methods &amp;amp; Procedure for Gathering Evidence (Wider Audit Methods)*&lt;/li&gt;&lt;li&gt;Interviewing and Writing Audit Findings&lt;/li&gt;&lt;li&gt;Handling and Managing Difficult Situations&lt;/li&gt;&lt;li&gt;Auditing Reporting (In more depth)**&lt;/li&gt;&lt;li&gt;Audit Findings, Terminology, Classification and Elements&lt;/li&gt;&lt;li&gt;Writing Audit Findings &amp;amp; the Audit Report&lt;/li&gt;&lt;li&gt;Completing the Audit&lt;/li&gt;&lt;li&gt;Audit Follow-Up Strategies (In-depth)**&lt;/li&gt;&lt;li&gt;Corrective&amp;nbsp;and Preventative Action including Audit Finding Closure (Robust Evaluation)**&lt;/li&gt;&lt;li&gt;Audit Follow Up Closing/Exit Meeting (Real Life Scenario)**&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;ul&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;span&gt;IRCA Certified Course (A18113)&lt;/span&gt;&lt;/h4&gt;
				&lt;div class=&quot;course_certification_logo&quot;&gt;
					&lt;p&gt;
						&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/cqi and irca course.png&quot; style=&quot;width: 250px;&quot;&gt;&lt;/p&gt;
				&lt;/div&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully recognised by CQI &amp;amp; IRCA.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Assessment of Process Effectiveness&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					To have a high performing QMS that directly and indirectly impacts business performance requires a QMS that is integrated with the organizations business processes.&lt;/p&gt;
				&lt;p&gt;
					Our course focuses on providing Learners with skills to provide real value and underpin Process Owner and other Stakeholder confidence – this leads to better improvements, more insightful audits, better quality information and therefore, better informed decisions.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Wider Coverage of Audit Methods&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					What sets the Kelmac Group® course apart from both the IRCA course specification and competitor courses is we develop the Learner’s competencyusing a wide variety of audit methods, namely interview, document review and analysis of process and product data and information and operational records.&lt;/p&gt;
				&lt;p&gt;
					By comparison, competitor courses only focus on one audit method, interview and this does not expose the QMS Auditor to the real-life audit situation – the Kelmac Group course does.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => Internal EMS Auditor based on ISO 14001:2015 Training Course
            [title_name] => Internal EMS Auditor based on ISO 14001:2015 Training Course | Kelmac Group UK
            [cert_name] => Internal EMS Auditor based on ISO 14001:2015 Training Course
            [cert_name_line1] => 
            [cert_name_line2] => 
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	The focus of the Kelmac Group® ISO 14001:2015 Internal Auditor Training Course is to provide Internal Auditors with both the confidence and ability to apply the audit assurance tools and techniques, methodology &amp;amp; desired behaviors to assess the organization’s EMS processes &amp;amp; process controls &lt;strong&gt;to consistently deliver environmental performance results that meet interested party and applicable statutory and regulatory requirements.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;
	We work on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of a EMS based on ISO 14001:2015 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an EMS, covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviours.&lt;/p&gt;
&lt;p&gt;
	&lt;br /&gt;
	&amp;nbsp;&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the Kelmac Group® ISO 14001:2015 Internal Auditor Training Course is to provide Internal Auditors with both the confidence and ability to apply the audit assurance tools and techniques, methodology &amp;amp; desired behaviors to assess the organization’s EMS processes &amp;amp; process controls &lt;strong&gt;to consistently deliver environmental performance results that meet interested party and applicable statutory and regulatory requirements.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;
	We work on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of a EMS based on ISO 14001:2015 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an EMS, covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behaviours.&lt;/p&gt;
&lt;p&gt;
	&lt;br /&gt;
	&amp;nbsp;&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	We focus on consistent interpretation &amp;amp; application the requirements of ISO 14001:2015 and the ability to plan, conduct, report and follow up an audit of a&lt;br /&gt;
	different Environmental Management System scenarios to provide Assurance the Environmental Management System meets the needs of the interested parties.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 5-day (45hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 18:00pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO 14001:2015 Requirements or have completed a recognised EMS Fundamentals course based on ISO 14001:2015 prior to registering for this course.&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Introduction to Internal Auditing&lt;/li&gt;
						&lt;li&gt;
							The role of Internal Audits and the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology and Principles&lt;/li&gt;
						&lt;li&gt;
							Audit Types and Objectives&lt;/li&gt;
						&lt;li&gt;
							Understanding the PDCA Cycle and Process Approach and their significance for Internal Auditors**&lt;/li&gt;
						&lt;li&gt;
							Internal Auditor Competence, Roles &amp;amp; Responsibilities&lt;/li&gt;
						&lt;li&gt;
							Behaviours &amp;amp; Performance Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Business Process Management**&lt;/li&gt;
						&lt;li&gt;
							Audit Planning (Process &amp;amp; Risk-based)**&lt;/li&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the on-site activities**&lt;/li&gt;
						&lt;li&gt;
							Developing an Audit Plan/Scope Audit Protocol (Checklist/Process Documentation)**&lt;/li&gt;
						&lt;li&gt;
							On-Site Audit Activities (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Opening Meeting (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Evidence, Methods &amp;amp; Procedure for Gathering Evidence (Wider Audit Methods)**&lt;/li&gt;
						&lt;li&gt;
							Interviewing and Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Handling and Managing Difficult Situations&lt;/li&gt;
						&lt;li&gt;
							Auditing Reporting (In more depth)**&lt;/li&gt;
						&lt;li&gt;
							Audit Findings, Terminology, Classification and Elements&lt;/li&gt;
						&lt;li&gt;
							Writing Audit Findings &amp;amp; the Audit Report&lt;/li&gt;
						&lt;li&gt;
							Completing the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up Strategies (In-depth)**&lt;/li&gt;
						&lt;li&gt;
							Corrective and Preventative Action including Audit Finding Closure (Robust Evaluation)**&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting (Real Life Scenario)**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => 
            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
	&lt;/div&gt;
&lt;/div&gt;
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            [right_alt] => iso 27001 internal auditor training certification uk
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            [name] => Internal ISMS Auditor based on ISO 27001 Training Course
            [title_name] => Internal ISMS Auditor based on ISO 27001 Training Course | Information Security | Kelmac Group UK
            [cert_name] => Internal ISMS Auditor based on ISO/IEC 27001:2013 Training Course
            [cert_name_line1] => 
            [cert_name_line2] => 
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	The focus of the &lt;strong&gt;ISO 27001 Internal Auditor&amp;nbsp;Training Course&lt;/strong&gt; is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of an ISMS based on ISO/IEC 27001:2013 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	&lt;strong&gt;During the delivery, the Learner will complete a Consultant facilitated audit of a process within an ISMS,&lt;/strong&gt; covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behavior&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the &lt;strong&gt;ISO 27001 Internal Auditor&amp;nbsp;Training Course&lt;/strong&gt; is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of an ISMS based on ISO/IEC 27001:2013 requirements with specific emphasis of 1st Party auditing [Internal audits].&lt;/p&gt;
&lt;p&gt;
	&lt;strong&gt;During the delivery, the Learner will complete a Consultant facilitated audit of a process within an ISMS,&lt;/strong&gt; covering the full audit life cycle as defined by ISO 19011 &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behavior&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Provides Internal Auditors with both the confidence and ability to apply the audit assurance tools &amp;amp; techniques, methodology and desired behaviors to assess the organization’s ISMS processes &amp;amp; process controls to &lt;strong&gt;consistent-ly preserve the confidentiality, integrity and availability of the organization’s information assets and give confidence to interested parties that risks are adequately managed.&lt;/strong&gt;&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 2-day (16hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day)&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO/IEC 27001:2013 Requirements or have received ISO/IEC 27001 Fundamentals training in advance of attending this course.&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Introduction to Internal Auditing&lt;/li&gt;
						&lt;li&gt;
							The role of Internal Audits and the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology and Principles&lt;/li&gt;
						&lt;li&gt;
							Audit Types and Objectives&lt;/li&gt;
						&lt;li&gt;
							Understanding the PDCA Cycle and Process Approach and their significance for Internal Auditors**&lt;/li&gt;
						&lt;li&gt;
							Internal Auditor Competence, Roles &amp;amp; Responsibilities&lt;/li&gt;
						&lt;li&gt;
							Behaviours &amp;amp; Performance Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Business Process Management**&lt;/li&gt;
						&lt;li&gt;
							Audit Planning (Process &amp;amp; Risk-based)**&lt;/li&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the on-site activities**&lt;/li&gt;
						&lt;li&gt;
							Developing an Audit Plan/Scope Audit Protocol (Checklist/Process Documentation)**&lt;/li&gt;
						&lt;li&gt;
							On-Site Audit Activities (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Opening Meeting (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Evidence, Methods &amp;amp; Procedure for Gathering Evidence (Wider Audit Methods)**&lt;/li&gt;
						&lt;li&gt;
							Interviewing and Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Handling and Managing Difficult Situations&lt;/li&gt;
						&lt;li&gt;
							Auditing Reporting (In more depth)**&lt;/li&gt;
						&lt;li&gt;
							Audit Findings, Terminology, Classification and Elements&lt;/li&gt;
						&lt;li&gt;
							Writing Audit Findings &amp;amp; the Audit Report&lt;/li&gt;
						&lt;li&gt;
							Completing the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up Strategies (In-depth)**&lt;/li&gt;
						&lt;li&gt;
							Corrective and Preventative Action including Audit Finding Closure (Robust Evaluation)**&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting (Real Life Scenario)**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Assessment of Process Effectiveness&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					To have a high performing ISMS that directly and indirectly impacts business performance requires a ISMS that is integrated with the organizations business processes.&lt;/p&gt;
				&lt;p&gt;
					Our course focuses on providing Learners with skills to provide real value and underpin Process Owner and other Stakeholder confidence – this leads to better improvements, more insightful audits, better quality information and therefore, better informed decisions.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Wider Coverage of Audit Methods&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					What sets the Kelmac Group® course apart from both the IRCA course specification and competitor courses is we develop the Learner’s competency using a wide variety of audit methods, namely interview, document review and analysis of process and product data and information and operational records.&lt;/p&gt;
				&lt;p&gt;
					By comparison, competitor courses only focus on one audit method, interview and this does not expose the ISMS Auditor to the real-life audit situation – the Kelmac Group course does.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
	&lt;/div&gt;
&lt;/div&gt;
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            [right_alt] => ohsas 18001 internal auditor courses uk
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            [review_coursecat_id] => 
            [name] => Internal OHS Auditor based on OHSAS 18001 Training Course
            [title_name] => Internal OHS Auditor based on OHSAS 18001 Training Course | Health &amp; Safety Internal Auditor | Kelmac Group UK
            [cert_name] => Internal OHS Auditor based on OHSAS 18001 Training Course
            [cert_name_line1] => 
            [cert_name_line2] => 
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	The focus of the Kelmac Group® OHSAS 18001 Internal Auditor Classroom Learning Course is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of a OH&amp;amp;SMS based on OHSAS 18001 requirements with specific emphasis of 1st Party auditing [Internal audits].&amp;nbsp;&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an OH&amp;amp;SMS, covering the full audit life cycle as defined by ISO 19011&amp;nbsp; &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behav&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	The focus of the Kelmac Group® OHSAS 18001 Internal Auditor Classroom Learning Course is on assisting and verifying the competencies &amp;amp; capabilities of the Learner to be able to effectively audit a process, activity or department/function of a OH&amp;amp;SMS based on OHSAS 18001 requirements with specific emphasis of 1st Party auditing [Internal audits].&amp;nbsp;&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated audit of a process within an OH&amp;amp;SMS, covering the full audit life cycle as defined by ISO 19011&amp;nbsp; &amp;amp; the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, auditor skills and behav&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Provide Internal Auditors with both the confidence and ability to apply the audit assurance tools and techniques, methodology and desired behaviors to assess the organization’s OH&amp;amp;S processes and process controls to consistently deliver occupational &lt;strong&gt;health and safety performance results that meet interested party and applicable statutory and regulatory requirements.&lt;/strong&gt;&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 2-day (16hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day)&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with OHSAS 18001:2007 Requirements or have received OHSAS 18001:2007 Fundamentals training in advance of attending this course.&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Introduction to Internal Auditing&lt;/li&gt;
						&lt;li&gt;
							The role of Internal Audits and the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology and Principles&lt;/li&gt;
						&lt;li&gt;
							Audit Types and Objectives&lt;/li&gt;
						&lt;li&gt;
							Understanding the PDCA Cycle and Process Approach and their significance for Internal Auditors**&lt;/li&gt;
						&lt;li&gt;
							Internal Auditor Competence, Roles &amp;amp; Responsibilities&lt;/li&gt;
						&lt;li&gt;
							Behaviours &amp;amp; Performance Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Business Process Management**&lt;/li&gt;
						&lt;li&gt;
							Audit Planning (Process &amp;amp; Risk-based)**&lt;/li&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the on-site activities**&lt;/li&gt;
						&lt;li&gt;
							Developing an Audit Plan/Scope Audit Protocol (Checklist/Process Documentation)**&lt;/li&gt;
						&lt;li&gt;
							On-Site Audit Activities (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Opening Meeting (Real Life Scenario)**&lt;/li&gt;
						&lt;li&gt;
							Evidence, Methods &amp;amp; Procedure for Gathering Evidence (Wider Audit Methods)**&lt;/li&gt;
						&lt;li&gt;
							Interviewing and Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Handling and Managing Difficult Situations&lt;/li&gt;
						&lt;li&gt;
							Auditing Reporting (In more depth)**&lt;/li&gt;
						&lt;li&gt;
							Audit Findings, Terminology, Classification and Elements&lt;/li&gt;
						&lt;li&gt;
							Writing Audit Findings &amp;amp; the Audit Report&lt;/li&gt;
						&lt;li&gt;
							Completing the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up Strategies (In-depth)**&lt;/li&gt;
						&lt;li&gt;
							Corrective and Preventative Action including Audit Finding Closure (Robust Evaluation)**&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting (Real Life Scenario)**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best?&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Assessment of Process Effectiveness&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					To have a high performing OH&amp;amp;SMS that directly and indirectly impacts business performance requires a OH&amp;amp;SMS&amp;nbsp; that is integrated with the organizations business processes. Our course focuses on providing Learners with skills to provide real value and underpin Process Owner and other Stakeholder confidence – this leads to better improvements, more insightful audits, better quality information and therefore, better informed decisions.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Wider Coverage of Audit Methods&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					What sets the Kelmac Group® course apart from both the IRCA course specification and competitor courses is we develop the Learner’s competency using a wide variety of audit methods, namely interview, document review and analysis of process and product data and information and operational records. By comparison, competitor courses only focus on one audit method, interview and this does not expose the OH&amp;amp;SMS&amp;nbsp; Auditor to the real-life audit situation – the Kelmac Group course does.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
	&lt;/div&gt;
&lt;/div&gt;
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            [name] => ISO 45001:2018 Lead Auditor Certification Training Course | CQI, IRCA Certified
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            [name] => FSMS Lead Auditor based on ISO 22000:2018 Training Course | Kelmac Group approved
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            [cert_name_line1] => FSMS Auditor/Lead Auditor based on
            [cert_name_line2] => ISO 22000:2018 Training Course
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            [cat_desc] => &lt;p&gt;We offer a comprehensive, highly interactive five-day&lt;strong&gt;&amp;nbsp;ISO 22000:2018 Lead Auditor Training&lt;/strong&gt;&amp;nbsp;C&lt;strong&gt;ourse&amp;nbsp;&lt;/strong&gt;that teaches students the principles, processes, and techniques used for the assessment of and management of Food Safety Hazards; and their significance for FSMS lead auditors.&lt;/p&gt;&lt;p&gt;Kelmac Group are the oldest IRCA Accredited Training Provider of ISO 22000 Lead Auditor training in the world since 2005. We have unmatched experience in this field that has seen us deliver this training in over 15 countries around the world and to some of the largest organizations in the world.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot;&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;We offer a comprehensive, highly interactive five-day&lt;strong&gt;&amp;nbsp;Kelmac Group approved ISO 22000:2018 Lead Auditor Training&lt;/strong&gt;&amp;nbsp;&lt;strong&gt;Course &lt;/strong&gt;that teaches students the principles, processes, and techniques used for the assessment of and management of Food Safety Hazards; and their significance for FSMS lead auditors.&lt;/p&gt;&lt;p&gt;Kelmac Group are the oldest IRCA Accredited Training Provider of ISO 22000 Lead Auditor training in the world since 2005. We have unmatched experience in this field that has seen us deliver this training in over 15 countries around the world and to some of the largest organizations in the world.&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;&lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot;&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	We focus on consistent interpretation &amp;amp; application the requirements of &lt;strong&gt;ISO 22000:2018&lt;/strong&gt; and the ability to plan, conduct, report and follow up an audit of different Food Safety Management System scenarios to provide Assurance the Food Safety Management System meets the needs of the interested parties.&lt;/p&gt;
&lt;/div&gt;
&lt;div class=&quot;six-step&quot;&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot;&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul style=&quot;list-style-type: square;&quot;&gt;
	&lt;li&gt;
		This is a 5-day (40hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
	&lt;li&gt;Prior Learning Requirements: There are&amp;nbsp;&lt;b&gt;&lt;u&gt;important&lt;/u&gt;&lt;/b&gt;&amp;nbsp;pre-requisites, please review the&amp;nbsp;&lt;u&gt;Course Overview&lt;/u&gt;&amp;nbsp;tab below to review these important details. &lt;/li&gt;&lt;li&gt;&lt;b&gt;Please note:&lt;/b&gt; by registering for this course, each Learner is confirming that they have read and fulfill any relevant prior learning requirements for this course:&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;&lt;div class=&quot;row gray-bg&quot;&gt;&lt;div class=&quot;container clearfix&quot;&gt;&lt;div class=&quot;course-learning clearfix&quot;&gt;&lt;div class=&quot;course-learning-title&quot;&gt;&lt;img src=&quot;https://www.kelmacgroup.com/admin/images/accrediation.jpg&quot;&gt;&amp;nbsp;Course Learning TopicsWhat does the course cover?&lt;/div&gt;&lt;ul class=&quot;clearfix&quot;&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;p&gt;&lt;strong&gt;Introduction to Food Safety Management Systems (FSMS)&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;What is an FSMS&lt;/li&gt;&lt;li&gt;ISO 22000 Family of Standards&lt;/li&gt;&lt;li&gt;Purpose, Benefits &amp;amp; Scope of ISO 22000:2018&lt;/li&gt;&lt;li&gt;Structure of ISO 22000:2018**&lt;/li&gt;&lt;li&gt;ISO 22000:2018 Terminology&lt;/li&gt;&lt;li&gt;Key Concepts underpinning ISO 22000:2018**&lt;/li&gt;&lt;li&gt;HACCP**&lt;/li&gt;&lt;li&gt;CCP, O-PRPs, PRPs**&lt;/li&gt;&lt;li&gt;Industry Sector Pre-Requisite Programs&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;strong&gt;Introduction to FSMS Auditing&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Types of Management System Audits&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Audit Terminology&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Audit Lifecycle**&lt;/li&gt;&lt;li&gt;Audit Team and Auditee Roles&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Desired Auditor Behaviours&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Audit Program Management**&lt;/li&gt;&lt;li&gt;Conformity Assessment Standards&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;p&gt;&lt;strong&gt;Initiation and Preparation for the Onsite Audit&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;&lt;li&gt;Establish contact with the auditee**&lt;/li&gt;&lt;li&gt;Audit scope, criteria, objectives&lt;/li&gt;&lt;li&gt;Audit Feasibility**&lt;/li&gt;&lt;li&gt;Audit working documents&lt;/li&gt;&lt;li&gt;Document review prior to onsite audit&lt;/li&gt;&lt;li&gt;Development of audit plan and audit checklists&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;strong&gt;Conducting the Onsite Audit&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Opening Meeting including Role Play&lt;/li&gt;&lt;li&gt;Gathering Evidence&lt;/li&gt;&lt;li&gt;Five Core Audit Methods**&lt;/li&gt;&lt;li&gt;Audit Sampling**&lt;/li&gt;&lt;li&gt;Management of the audit team&lt;/li&gt;&lt;li&gt;Communication throughout the audit&lt;/li&gt;&lt;li&gt;Handling Auditee Reactions**&lt;/li&gt;&lt;li&gt;Live Simulated Audit of a documented FSMS&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;b&gt;Audit Reporting&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Audit Finding Reporting&lt;/li&gt;&lt;li&gt;Audit Report and Conclusion&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;p&gt;&lt;b&gt;Final Audit Team and Closing/Exit Meeting&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Final Audit Team Meeting**&lt;/li&gt;&lt;li&gt;Closing/Exit Meeting&lt;/li&gt;&lt;li&gt;Audit Follow Up including Evaluation of Corrective Actions&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;&lt;div class=&quot;course_certification_terms&quot;&gt;&lt;/div&gt;&lt;div class=&quot;course_certification&quot;&gt;&lt;img class=&quot;img_left&quot; src=&quot;https://www.kelmacgroup.com/admin/images/certificate-icon.jpg&quot;&gt;&lt;h4&gt;Course Certification Kelmac Group approved&lt;/h4&gt;&lt;div class=&quot;course_certification_logo&quot;&gt;&lt;/div&gt;&lt;div class=&quot;course_certification_description&quot;&gt;&lt;!---&lt;p&gt;This course has become the first course in the world to be certified by CQI &amp;amp; IRCA in ISO 22000:2018.&lt;/p&gt;---&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot;&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented FSMS&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented FSMS from the unique Kelmac Group assurance perspective. The Kelmac Group assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&lt;/p&gt;
				&lt;p&gt;
					Our almost fully documented Dairy [Milk Processing] FSMS includes a Food Safety Policy Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; a Dairy Milk Processing HACCP System, the organization’s statutory and regulatory and other legal obligations register, the organization’s emergency preparedness and response plan, food defense plan, the organization’s risk register, and related documented FSMS templates and records. The comprehensive case study truly places Kelmac Group at the top of the market.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;&lt;br&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [right_alt] => iso 22000 lead auditor training certification uk
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            [name] => FSMS Lead Auditor based on ISO 22000:2018 Training Course | CQI &amp; IRCA Certified
            [title_name] => FSMS Lead Auditor based on ISO 22000:2018 Training Course | CQI &amp; IRCA Certified
            [cert_name] => 
            [cert_name_line1] => FSMS Auditor/Lead Auditor based on
            [cert_name_line2] => ISO 22000:2018 Training Course
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            [cat_desc] => &lt;p&gt;We offer a comprehensive, highly interactive five-day&lt;strong&gt;&amp;nbsp;ISO 22000:2018 Lead Auditor Training&lt;/strong&gt;&amp;nbsp;C&lt;strong&gt;ourse (&lt;/strong&gt;&lt;strong&gt;CQI and IRCA Certification Pending)&amp;nbsp;&lt;/strong&gt;that teaches students the principles, processes, and techniques used for the assessment of and management of Food Safety Hazards; and their significance for FSMS lead auditors.&lt;/p&gt;&lt;p&gt;Kelmac Group are the oldest IRCA Accredited Training Provider of ISO 22000 Lead Auditor training in the world since 2005. We have unmatched experience in this field that has seen us deliver this training in over 15 countries around the world and to some of the largest organizations in the world.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot;&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;We offer a comprehensive, highly interactive five-day&lt;strong&gt;&amp;nbsp;CQI &amp;amp; IRCA Certified ISO 22000:2018 Lead Auditor Training&lt;/strong&gt;&amp;nbsp;C&lt;strong&gt;ourse (&lt;/strong&gt;&lt;strong&gt;CQI and IRCA Certification Pending)&amp;nbsp;&lt;/strong&gt;that teaches students the principles, processes, and techniques used for the assessment of and management of Food Safety Hazards; and their significance for FSMS lead auditors.&lt;/p&gt;&lt;p&gt;Kelmac Group are the oldest IRCA Accredited Training Provider of ISO 22000 Lead Auditor training in the world since 2005. We have unmatched experience in this field that has seen us deliver this training in over 15 countries around the world and to some of the largest organizations in the world.&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;&lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot;&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	We focus on consistent interpretation &amp;amp; application the requirements of &lt;strong&gt;ISO 22000:2018&lt;/strong&gt; and the ability to plan, conduct, report and follow up an audit of different Food Safety Management System scenarios to provide Assurance the Food Safety Management System meets the needs of the interested parties.&lt;/p&gt;
&lt;/div&gt;
&lt;div class=&quot;six-step&quot;&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot;&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul style=&quot;list-style-type: square;&quot;&gt;
	&lt;li&gt;
		This is a 5-day (40hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
	&lt;li&gt;Prior Learning Requirements: There are&amp;nbsp;&lt;b&gt;&lt;u&gt;important&lt;/u&gt;&lt;/b&gt;&amp;nbsp;pre-requisites, please review the&amp;nbsp;&lt;u&gt;Course Overview&lt;/u&gt;&amp;nbsp;tab below to review these important details. &lt;/li&gt;&lt;li&gt;&lt;b&gt;Please note:&lt;/b&gt; by registering for this course, each Learner is confirming that they have read and fulfill any relevant prior learning requirements for this course:&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;&lt;div class=&quot;row gray-bg&quot;&gt;&lt;div class=&quot;container clearfix&quot;&gt;&lt;div class=&quot;course-learning clearfix&quot;&gt;&lt;div class=&quot;course-learning-title&quot;&gt;&lt;img src=&quot;https://www.kelmacgroup.com/admin/images/accrediation.jpg&quot;&gt;&amp;nbsp;Course Learning TopicsWhat does the course cover?&lt;/div&gt;&lt;ul class=&quot;clearfix&quot;&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;p&gt;&lt;strong&gt;Introduction to Food Safety Management Systems (FSMS)&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;What is an FSMS&lt;/li&gt;&lt;li&gt;ISO 22000 Family of Standards&lt;/li&gt;&lt;li&gt;Purpose, Benefits &amp;amp; Scope of ISO 22000:2018&lt;/li&gt;&lt;li&gt;Structure of ISO 22000:2018**&lt;/li&gt;&lt;li&gt;ISO 22000:2018 Terminology&lt;/li&gt;&lt;li&gt;Key Concepts underpinning ISO 22000:2018**&lt;/li&gt;&lt;li&gt;HACCP**&lt;/li&gt;&lt;li&gt;CCP, O-PRPs, PRPs**&lt;/li&gt;&lt;li&gt;Industry Sector Pre-Requisite Programs&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;strong&gt;Introduction to FSMS Auditing&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Types of Management System Audits&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Audit Terminology&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Audit Principles** &amp;amp; CQI and IRCA Code of Conduct&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Audit Lifecycle**&lt;/li&gt;&lt;li&gt;Audit Team and Auditee Roles&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Desired Auditor Behaviours&lt;/li&gt;&lt;li&gt;ISO 19011:2018 Audit Program Management**&lt;/li&gt;&lt;li&gt;Conformity Assessment Standards&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;p&gt;&lt;strong&gt;Initiation and Preparation for the Onsite Audit&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;&lt;li&gt;Establish contact with the auditee**&lt;/li&gt;&lt;li&gt;Audit scope, criteria, objectives&lt;/li&gt;&lt;li&gt;Audit Feasibility**&lt;/li&gt;&lt;li&gt;Audit working documents&lt;/li&gt;&lt;li&gt;Document review prior to onsite audit&lt;/li&gt;&lt;li&gt;Development of audit plan and audit checklists&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;strong&gt;Conducting the Onsite Audit&lt;/strong&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Opening Meeting including Role Play&lt;/li&gt;&lt;li&gt;Gathering Evidence&lt;/li&gt;&lt;li&gt;Five Core Audit Methods**&lt;/li&gt;&lt;li&gt;Audit Sampling**&lt;/li&gt;&lt;li&gt;Management of the audit team&lt;/li&gt;&lt;li&gt;Communication throughout the audit&lt;/li&gt;&lt;li&gt;Handling Auditee Reactions**&lt;/li&gt;&lt;li&gt;Live Simulated Audit of a documented FSMS&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;b&gt;Audit Reporting&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Audit Finding Reporting&lt;/li&gt;&lt;li&gt;Audit Report and Conclusion&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;p&gt;&lt;b&gt;Final Audit Team and Closing/Exit Meeting&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Final Audit Team Meeting**&lt;/li&gt;&lt;li&gt;Closing/Exit Meeting&lt;/li&gt;&lt;li&gt;Audit Follow Up including Evaluation of Corrective Actions&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;&lt;div class=&quot;course_certification_terms&quot;&gt;&lt;p&gt;&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the CQI &amp;amp; IRCA specification&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;course_certification&quot;&gt;&lt;img class=&quot;img_left&quot; src=&quot;https://www.kelmacgroup.com/admin/images/certificate-icon.jpg&quot;&gt;&lt;h4&gt;Course CertificationCQI and IRCA Certified (1981)&lt;/h4&gt;&lt;div class=&quot;course_certification_logo&quot;&gt;&lt;/div&gt;&lt;div class=&quot;course_certification_description&quot;&gt;&lt;p&gt;This course has become the first course in the world to be certified by CQI &amp;amp; IRCA in ISO 22000:2018.&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot;&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented FSMS&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented FSMS from the unique Kelmac Group assurance perspective. The Kelmac Group assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&lt;/p&gt;
				&lt;p&gt;
					Our almost fully documented Dairy [Milk Processing] FSMS includes a Food Safety Policy Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; a Dairy Milk Processing HACCP System, the organization’s statutory and regulatory and other legal obligations register, the organization’s emergency preparedness and response plan, food defense plan, the organization’s risk register, and related documented FSMS templates and records. The comprehensive case study truly places Kelmac Group at the top of the market.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;&lt;br&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [min_grade_final_exam_option] => 1
            [delivery_type] => Blended
            [show_at_menu] => Yes
            [image_tag] => 
            [cf_title] => 
            [background_image] => 
            [cfft_desc] => 
            [language_id] => 1
            [review_course_id] => 
            [review_coursecat_id] => 
            [name] => ISO 13485:2016 Lead Auditor Certification Training Course - Kelmac Group approved
            [title_name] => ISO 13485:2016 Lead Auditor Certification Training Course - Kelmac Group approved
            [cert_name] => 
            [cert_name_line1] => QMS Auditor/Lead Auditor
            [cert_name_line2] => incorporating the requirements of
            [cert_name_line3] => ISO 13485:2016 Training Course
            [cat_desc] => &lt;p&gt;
	This &lt;strong&gt;ISO 13485:2016 Lead Auditor Training Course &lt;/strong&gt;[Quality Auditor/Lead Auditor incorporating the requirements of ISO 13485:2016 Training Course]&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete QMS based on ISO 13485 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing &amp;nbsp;[Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	&lt;strong&gt;During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a QMS [Medical Devices].&lt;/strong&gt; The facilitated audit of the QMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot;&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This &lt;strong&gt;Quality Management Systems Auditor/Lead Auditor Training Course (incorporating the requirements of ISO 13485:2016)&lt;/strong&gt;&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete QMS based on ISO 13485 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing &amp;nbsp;[Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	&lt;strong&gt;During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a QMS [Medical Devices].&lt;/strong&gt; The facilitated audit of the QMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques.&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;
	&lt;h4&gt;
		&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
	&lt;p&gt;
		With an&lt;strong&gt; additional 5 hours of learning&lt;/strong&gt; compared to our competitors, we cover new and additional topics in more depth. We focus on auditing that &lt;strong&gt;provides Assurance&lt;/strong&gt; that the Quality Management System meets the needs of the interested parties &amp;amp; our Learners are equipped to make &lt;strong&gt;&amp;nbsp;higher quality insights for improved organizational performance.&lt;/strong&gt;&lt;/p&gt;
&lt;/div&gt;
&lt;div class=&quot;six-step&quot;&gt;
	&lt;h4&gt;
		&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
	&lt;ul&gt;
		&lt;li&gt;
			This is a 5-day (45hr) learning event.&lt;/li&gt;
		&lt;li&gt;
			Start/Finish Times: 08:00am – 18:00pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
		&lt;li&gt;
			Prior Learning Requirement: Learners are required to be familiar with ISO 13485:2016 Requirements or have completed a recognised QMS Fundamentals course based on ISO 13485:2016 prior to registering for this course.&lt;/li&gt;
	&lt;/ul&gt;
&lt;/div&gt;
&lt;br /&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to Auditing&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Terminology, Principles, QMS Audits&lt;/li&gt;
						&lt;li&gt;
							Auditor Code of Ethics&lt;/li&gt;
						&lt;li&gt;
							Management of an Audit Program&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology, Principles, QMS Audits&lt;/li&gt;
						&lt;li&gt;
							Audit Life Cycle (On-site &amp;amp; Off-site Audit Activities)&lt;/li&gt;
						&lt;li&gt;
							Auditor/Auditee Roles, Responsibilities*&lt;/li&gt;
						&lt;li&gt;
							Desired Auditor Behaviours**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to QMS Auditing &lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Process Terminology*&lt;/li&gt;
						&lt;li&gt;
							Process Models/Methodology &amp;amp; Categories*&lt;/li&gt;
						&lt;li&gt;
							Evaluation of the effectiveness of a Process*&lt;/li&gt;
						&lt;li&gt;
							Processes and the application of PDCA and Risk*&lt;/li&gt;
						&lt;li&gt;
							The QMS Certification Cycle &amp;amp; 3rd Party Certification**&lt;/li&gt;
						&lt;li&gt;
							Special Conformity Audits**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Compliance Auditing &amp;amp; Methodology**&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Medical Device Life Cycle &amp;amp; the Regulatory Audit Perspective**&lt;/li&gt;
						&lt;li&gt;
							Overview of Different Regulatory Requirements [EU, U.S, Japan, Canada &amp;amp; More]**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Trails&lt;/li&gt;
						&lt;li&gt;
							Purpose and benefits for establishing initial contact and forms of contact&lt;/li&gt;
						&lt;li&gt;
							Case Study: Document Review&lt;/li&gt;
						&lt;li&gt;
							Audit Plan&lt;/li&gt;
						&lt;li&gt;
							Audit Checklist&lt;/li&gt;
						&lt;li&gt;
							Audit Protocol&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Onsite Activities&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Lead Auditor Leadership and Supervision**&lt;/li&gt;
						&lt;li&gt;
							Responsibilities of the Lead Auditor&lt;/li&gt;
						&lt;li&gt;
							Communication throughout the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Monitoring Audit Progress&lt;/li&gt;
						&lt;li&gt;
							Consensus and Resolution Conflicts&lt;/li&gt;
						&lt;li&gt;
							Lead Auditor Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Reporting&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up&lt;/li&gt;
						&lt;li&gt;
							Auditor/Technical Expert Coaching, Mentoring and Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Collecting and Verifying Information&lt;/li&gt;
						&lt;li&gt;
							Introduction to Audit Findings&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Opening Meeting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Purpose, process and benefit of an Opening Meeting&lt;/li&gt;
						&lt;li&gt;
							Case Study – Opening Meeting&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Reporting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing the Audit Report**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Completing the Audit&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Evaluating Correction &amp;amp; Corrective Action including Root Cause Analysis and Audit Finding Closure&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up Strategies&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting &amp;amp; Role Play&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;span&gt;Kelmac Group approved&lt;/span&gt;&lt;/h4&gt;
				&lt;!---&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;div class=&quot;course_certification_description&quot;&gt;
						&lt;p&gt;&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/CQI-IRCA-Certified-ISO-134852016-Lead-Auditor-Certification-Training-Course-uk.png&quot; style=&quot;width: 250px;&quot;&gt;This course is fully recognized by CQI &amp;amp; IRCA.&lt;/p&gt;
					&lt;/div&gt;
				&lt;/div&gt;----&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented QMS for Medical Devices&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented QMS [MD] from the unique Kelmac Group® assurance perspective.&lt;/p&gt;
				&lt;p&gt;
					The &lt;strong&gt;Kelmac Group® assurance &lt;/strong&gt;&lt;strong&gt;perspective is unique&lt;/strong&gt; as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at &lt;strong&gt;improving performance of the organization.&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented QMS Case Study [Medical Devices] available in the market and provides the Learner with the mostrealistic practical audit experience available on the market including a ISO 13485 Quality Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; and related documented templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Evaluating Business Processes&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					An important USP of this Kelmac Group course is that we show each Learner how to evaluate &lt;strong&gt;business processes,&lt;/strong&gt; not just ISO processes and align with the strategic intent of the organization. Business Processes include Marketing &amp;amp; Sales, Design Control, Manufacturing, Logistics, Installation, Purchasing, Servicing &amp;amp; HR. We &lt;strong&gt;cover this practically&lt;/strong&gt; and from the QMS [MD] Auditor Perspective.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Live Audit Vs. Facilitated Audit&lt;span&gt;Which is better? Why?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Some competitors offer a “live” audit as part of their training. However a “live audit” of such short duration (&amp;lt;0.5 day typically) is of &lt;strong&gt;limited value&lt;/strong&gt; as the Learner does not get an opportunity to audit an almost fully documented QMS [Medical Devices].&lt;/p&gt;
				&lt;p&gt;
					Kelmac Group’s course includes a “facilitated” audit which enables us to truly &lt;strong&gt;verify the Learner’s core audit skills&lt;/strong&gt; through working with an almost fully documented Quality Management System [Medical Devices].&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br /&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [duration_days] => 5
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            [name] => OHSAS 18001 Lead Auditor Training Course | IRCA Certified
            [title_name] => OHSAS 18001 Lead Auditor Training Course | IRCA Certified
            [cert_name] =>  
            [cert_name_line1] => OHSMS Auditor/Lead Auditor based on
            [cert_name_line2] => OHSAS 18001:2007 Training Course
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;IRCA Certified OHSAS 18001 Lead Auditor Training&lt;/strong&gt;&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete OH&amp;amp;SMS based on OHSAS 18001:2007 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing [Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of an OH&amp;amp;SMS.&amp;nbsp; The facilitated audit of the OH&amp;amp;SMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective applica&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot;&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;IRCA Certified OHSAS 18001 Lead Auditor Training&lt;/strong&gt;&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete OH&amp;amp;SMS based on OHSAS 18001:2007 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing [Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of an OH&amp;amp;SMS.&amp;nbsp; The facilitated audit of the OH&amp;amp;SMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective applica&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot;&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Our training demonstrates to the Learner the benefits of adopting the unique Kelmac Group® &lt;strong&gt;One System Model&lt;/strong&gt; for enhancing organizational compliance, effectiveness and efficiency based on utilizing Business Process Management to enhance ISO.&lt;/p&gt;
&lt;br&gt;
&lt;br&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot;&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 1-day (8hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm&lt;/li&gt;
&lt;/ul&gt;
&lt;br&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Business/Societal Case for&amp;nbsp;OHSAS 18001:2007&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex SL&lt;/li&gt;
						&lt;li&gt;
							New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							The Relationship between External and Internal Issues, Interested Party Requirements&lt;/li&gt;
						&lt;li&gt;
							Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Leadership&lt;/li&gt;
						&lt;li&gt;
							Effective Communication and Life Cycle Thinking&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to Auditing&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Terminology, Principles, OHSMS Audits&lt;/li&gt;
						&lt;li&gt;
							Auditor Code of Ethics&lt;/li&gt;
						&lt;li&gt;
							Management of an Audit Program&lt;/li&gt;
						&lt;li&gt;
							Audit Life Cycle (On-site &amp;amp; Off-site Audit Activities)&lt;/li&gt;
						&lt;li&gt;
							Auditor/Auditee Roles, Responsibilities*&lt;/li&gt;
						&lt;li&gt;
							Desired Auditor Behaviours**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to OHSMS Auditing &lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Aligning the Business Processes and the OHSMS Model*&lt;/li&gt;
						&lt;li&gt;
							Process Terminology*&lt;/li&gt;
						&lt;li&gt;
							Process Models/Methodology &amp;amp; Categories*&lt;/li&gt;
						&lt;li&gt;
							Evaluation of the Effectiveness of a Process*&lt;/li&gt;
						&lt;li&gt;
							Processes and the Application of PDCA and Risk*&lt;/li&gt;
						&lt;li&gt;
							The OHSMS Certification Cycle &amp;amp; 3rd Party Certification**&lt;/li&gt;
						&lt;li&gt;
							Special Conformity Audits**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Trails&lt;/li&gt;
						&lt;li&gt;
							Purpose and benefits for establishing initial contact and forms of contact&lt;/li&gt;
						&lt;li&gt;
							Case Study: Document Review&lt;/li&gt;
						&lt;li&gt;
							Audit Plan&lt;/li&gt;
						&lt;li&gt;
							Audit Checklist&lt;/li&gt;
						&lt;li&gt;
							Audit Protocol&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Opening Meeting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Purpose, process and benefit of an Opening Meeting&lt;/li&gt;
						&lt;li&gt;
							Case Study – Opening Meeting&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Onsite Activities&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Lead Auditor Leadership and Supervision**&lt;/li&gt;
						&lt;li&gt;
							Responsibilities of the Lead Auditor&lt;/li&gt;
						&lt;li&gt;
							Communication throughout the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Monitoring Audit Progress&lt;/li&gt;
						&lt;li&gt;
							Consensus and Resolution Conflicts&lt;/li&gt;
						&lt;li&gt;
							Lead Auditor Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Reporting&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up&lt;/li&gt;
						&lt;li&gt;
							Auditor/Technical Expert Coaching, Mentoring and Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Collecting and Verifying Information&lt;/li&gt;
						&lt;li&gt;
							Introduction to Audit Findings&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Reporting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing the Audit Report**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Completing the Audit&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Evaluating Correction &amp;amp; Corrective Action including Root Cause Analysis and Audit Finding Closure&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up Strategies&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting &amp;amp; Role Play&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;span&gt;CQI &amp;amp; IRCA Certified Course (A17438)&lt;/span&gt;&lt;/h4&gt;
				&lt;div class=&quot;course_certification_logo&quot;&gt;
					&lt;p&gt;
						&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/cqi and irca course.png&quot; style=&quot;width: 250px;&quot;&gt;&lt;/p&gt;
				&lt;/div&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully recognised by CQI &amp;amp; IRCA.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot;&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? &lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented OHSMS &lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented ISMS from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented ISMS Case Study available including a Policy Manual; Statement of Applicability; Asset/Risk Register and Risk Treatment Plan, 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; the organization’s statutory and regulatory and other legal obligations register, and the organization’s risk register, and related documented Information Security templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					One System Model&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The one system model is based on utilizing Business Process Management to enhance ISO based Management Systems.&lt;/p&gt;
				&lt;p&gt;
					Our course is unlike our competitors as we will outline a methodology for developing and implementing an Information Security Management System based upon the requirements of OHSAS 18001:2007, where the OHSMS is integrated with the organization’s business model.&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Others train followers, we train leaders™&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					More Topics Covered In More Depth&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					In this course, we cover 14 topics in more depth than any of our competitors!&lt;/p&gt;
				&lt;p&gt;
					If you look at other courses, they are largely focused on knowledge based learning which does not cover all requirements of ISO 27001.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
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			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe src=&quot;https://player.vimeo.com/video/143114881&quot; height=&quot;222&quot; frameborder=&quot;0&quot; webkitallowfullscreen=&quot;&quot; mozallowfullscreen=&quot;&quot; allowfullscreen=&quot;&quot;&gt;&lt;/iframe&gt;
	&lt;/div&gt;
&lt;/div&gt;
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            [name] => ISO 9001:2015 Auditor Transition Training Course
            [title_name] => ISO 9001:2015 Auditor Transition Training | Quality Management Systems
            [cert_name] => ISO 9001:2015 Auditor Transition Training Course
            [cert_name_line1] => 
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            [cat_desc] => &lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;ISO 9001:2015 Auditor Transition Training Course&lt;/strong&gt;&amp;nbsp;is aimed at existing Auditors of Quality Management Systems disciplines who perform first, second and third-party audits of Quality Management Systems against ISO 9001, in accordance with ISO 19011 and ISO 17021, as applicable.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;ISO 9001:2015 Auditor Transition Training Course&lt;/strong&gt;&amp;nbsp;is aimed at existing Auditors of Quality Management Systems disciplines who perform first, second and third-party audits of Quality Management Systems against ISO 9001, in accordance with ISO 19011 and ISO 17021, as applicable.&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;&lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	With an &lt;strong&gt;additional 4 hours of Learning&lt;/strong&gt; compared to our competitors, we focus on the ability to plan, conduct, report and follow up an audit of different Quality Management Systems [QMS] to &lt;strong&gt;provide Assurance&lt;/strong&gt; the QMS meets the needs of the interested parties.&lt;/p&gt;
&lt;/div&gt;&lt;div class=&quot;six-step&quot;&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 2-day (18hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 18:00pm (each day)&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO 9001:2008 Requirements &amp;amp; have knowledge of management systems audit through satisfactory completion of an IRCA Certified Internal QMS Auditor or QMS Auditor/Lead Auditor Training course (or acceptable alternative)&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Purpose and impact of Annex SL, the Framework for a generic management system&lt;/li&gt;
						&lt;li&gt;
							New and revised Terminology&lt;/li&gt;
						&lt;li&gt;
							The relationship between external and internal issues, interested party requirements, risks and opportunities, top management and business processes**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 9001:2015 - Context of the Organization&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The new requirements for Context of the Organization&lt;/li&gt;
						&lt;li&gt;
							The Organizations External and Internal Issues, Interested Parties, their Needs, Significance&lt;/li&gt;
						&lt;li&gt;
							Monitoring and Measurement&lt;/li&gt;
						&lt;li&gt;
							The PDCA Cycle and the Process-based Quality Management System Model for ISO 9001:2015&lt;/li&gt;
						&lt;li&gt;
							The Organization Business Model, Alignment with the Quality Management System Process Model [BPMS] and Benefits**&lt;/li&gt;
						&lt;li&gt;
							Audit Methods, Evidence and Sources**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 9001:2015 - Leadership&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The new and enhanced requirements for Leadership&lt;/li&gt;
						&lt;li&gt;
							The Seven Principles of Quality Management*&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 9001:2015 - Planning of the QMS&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Planning of the Quality Management System&lt;/li&gt;
						&lt;li&gt;
							Risks and Opportunities**&lt;/li&gt;
						&lt;li&gt;
							Quality Objectives and Plans to achieve them*&lt;/li&gt;
						&lt;li&gt;
							Management of Change*&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 9001:2015 - Support&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The requirements for Support&lt;/li&gt;
						&lt;li&gt;
							The new and enhanced Requirements for Awareness and Communications&lt;/li&gt;
						&lt;li&gt;
							Annex SL requirements for documented information and how it differs from previous management system requirements&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 9001:2015 - Operation&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Operation&lt;/li&gt;
						&lt;li&gt;
							The new and enhanced Requirements for Operational Planning and Control, specifically Outsourcing&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 9001:2015 - Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Scope and Criteria of the Audit Audit Plan**&lt;/li&gt;
						&lt;li&gt;
							Case Study Review &amp;amp; Audit Protocol Development*&lt;/li&gt;
						&lt;li&gt;
							Conducting the On-Site Audit&lt;/li&gt;
						&lt;li&gt;
							Ability to manage Meetings [Opening Meeting]&lt;/li&gt;
						&lt;li&gt;
							Ability to Interview Top Management and Follow Audit Trails**&lt;/li&gt;
						&lt;li&gt;
							Audit Findings Simulated Audit/Case Study &amp;amp; Writing Audit Findings**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 9001:2015 - Audit Reporting &amp;amp; Preparing for and Managing the Closing-Exit Meeting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Report&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							Writing the Audit Report (Executive&amp;nbsp;Summary)*&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit&amp;nbsp;Meeting &amp;amp; Role Play&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented QMS&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented QMS from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented QMS Case Study available including a ISO 9001:2015 Quality Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; and related documented templates and records. In summary, our course unlike our competitors is based almost 100% on the practical application of effectively auditing to the requirement of ISO 9001:2015 rather than knowledge based learning.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Auditor Transition Training That Goes Further&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The additional learning topics we cover and the depth to which we cover these topics is why we added 4 hours of additional content.&lt;/p&gt;
				&lt;p&gt;
					We do not believe the learning objectives can be taught effectively in less time and have stuck by ethics and core principles to ensure we offer a learning event that is effective and our Learners will be able to practically apply the knowledge and skills after the training.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br /&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => ISO 14001:2015 Auditor Transition Training Course
            [title_name] => ISO 14001:2015 Auditor Transition Training Course | Kelmac Group UK
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            [cat_desc] => &lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;ISO 14001:2015 Auditor&amp;nbsp;Transition Training Course&lt;/strong&gt;&amp;nbsp;is aimed at existing Auditors of Environmental Management Systems disciplines who perform first, second and third-party audits of Environmental Management Systems against ISO 14001:2015, in accordance with ISO 19011 and ISO 17021, as applicable.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;ISO 14001:2015 Auditor&amp;nbsp;Transition Training Course&lt;/strong&gt;&amp;nbsp;is aimed at existing Auditors of Environmental Management Systems disciplines who perform first, second and third-party audits of Environmental Management Systems against ISO 14001:2015, in accordance with ISO 19011 and ISO 17021, as applicable.&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;&lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	With an additional 4 hours of Learning compared to our competitors, we focus on the ability to plan, conduct, report and follow up an audit of different Environmental Management Systems [EMS] to provide Assurance the EMS meets the needs of the interested parties.&lt;/p&gt;
&lt;/div&gt;&lt;div class=&quot;six-step&quot;&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 2-day (18hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 18:00pm (each day)&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO 14001:2004 Requirements &amp;amp; have knowledge of management systems audit through satisfactory completion of an IRCA Certified Internal EMS Auditor or EMS Auditor/Lead Auditor Training course (or acceptable alternative)&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The business/societal case for ISO 14001:2015**&lt;/li&gt;
						&lt;li&gt;
							Overview of ISO 14000 Standards Family*&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex SL New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							The Relationship between External and Internal Issues, Interested Party Requirements&lt;/li&gt;
						&lt;li&gt;
							Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Leadership&lt;/li&gt;
						&lt;li&gt;
							Effective Communication &amp;amp; Life Cycle Thinking&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Context of the Organization&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The New Requirements for Context of the Organization&lt;/li&gt;
						&lt;li&gt;
							The PDCA Cycle and the Process-based Environmental Management System Model for ISO 14001:2015**&lt;/li&gt;
						&lt;li&gt;
							The Organization Business Model, Alignment with the Environmental Management System Process Model [BPMS] and Benefits**&lt;/li&gt;
						&lt;li&gt;
							Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Leadership&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The new and enhanced requirements for Leadership&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Planning of the EMS&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Planning of the Environmental Management System&lt;br&gt;
							Risks and Opportunities*&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							EMS Objectives and Plans to achieve them* &amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							Management of Change*&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Support&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The requirements for Support&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							The new and enhanced Requirements for Awareness and Communications&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							Annex SL requirements for documented information and how it differs from previous management system requirements&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;ISO 14001:2015 - Operation&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Requirements for Operation&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							The new and enhanced Requirements for Operational Planning and Control, specifically Outsourcing&amp;nbsp;&lt;/li&gt;
						&lt;li&gt;
							Audit Evidence and Sources*&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Scope and Criteria of the Audit Audit Plan*&lt;/li&gt;
						&lt;li&gt;
							Case Study Review &amp;amp; Audit Protocol Development*&lt;/li&gt;
						&lt;li&gt;
							Conducting the On-Site Audit Ability to manage Meetings [Opening Meeting]&lt;/li&gt;
						&lt;li&gt;
							Ability to Interview Top Management and Follow Audit Trails*&lt;/li&gt;
						&lt;li&gt;
							Audit Findings Simulated Audit/Case Study &amp;amp; Writing Audit Findings*&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Reporting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Report&amp;nbsp;Writing the Audit Report (Executive&amp;nbsp;Summary)*&lt;/li&gt;
						&lt;li&gt;
							Preparing for and Managing the Closing-Exit Meeting&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit&amp;nbsp;Meeting &amp;amp; Role Play&amp;nbsp;&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;


            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented EMS&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented EMS from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented EMS Case Study available including an Integrated EHS (ISO 14001 &amp;amp; OHSAS 18001/ISO 45001) Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; the organization’s environmental aspects/impacts register, the organization’s statutory and regulatory and other legal obligations register, the organization’s emergency preparedness and response plan and the organization’s risk register, and related documented environmental templates and records.&lt;br /&gt;
					In summary, our course unlike our competitors is based almost 100% on the practical application of effectively auditing to the requirement of ISO 14001:2015 rather than knowledge based learning.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Auditor Transition Training That Goes Further&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The additional learning topics we cover and the depth to which we cover these topics is why we added 4 hours of additional content. We do not believe the learning objectives can be taught effectively in less time and have stuck by ethics and core principles to ensure we offer a learning event that is effective and our Learners will be able to practically apply the knowledge and skills after the training.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => ISO 13485:2016 Lead Auditor Certification Training Course - CQI &amp; IRCA Certified
            [title_name] => ISO 13485:2016 Lead Auditor Certification Training Course - CQI &amp; IRCA Certified
            [cert_name] => 
            [cert_name_line1] => QMS Auditor/Lead Auditor
            [cert_name_line2] => incorporating the requirements of
            [cert_name_line3] => ISO 13485:2016 Training Course
            [cat_desc] => &lt;p&gt;
	This &lt;strong&gt;ISO 13485:2016 Lead Auditor Training Course &lt;/strong&gt;[Quality Auditor/Lead Auditor incorporating the requirements of ISO 13485:2016 Training Course]&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete QMS based on ISO 13485 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing &amp;nbsp;[Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	&lt;strong&gt;During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a QMS [Medical Devices].&lt;/strong&gt; The facilitated audit of the QMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot;&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This &lt;strong&gt;Quality Management Systems Auditor/Lead Auditor Training Course (incorporating the requirements of ISO 13485:2016)&lt;/strong&gt;&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete QMS based on ISO 13485 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing &amp;nbsp;[Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	&lt;strong&gt;During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a QMS [Medical Devices].&lt;/strong&gt; The facilitated audit of the QMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques.&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;
	&lt;h4&gt;
		&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot;&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
	&lt;p&gt;
		With an&lt;strong&gt; additional 5 hours of learning&lt;/strong&gt; compared to our competitors, we cover new and additional topics in more depth. We focus on auditing that &lt;strong&gt;provides Assurance&lt;/strong&gt; that the Quality Management System meets the needs of the interested parties &amp;amp; our Learners are equipped to make &lt;strong&gt;&amp;nbsp;higher quality insights for improved organizational performance.&lt;/strong&gt;&lt;/p&gt;
&lt;/div&gt;
&lt;div class=&quot;six-step&quot;&gt;
	&lt;h4&gt;
		&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot;&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
	&lt;ul&gt;
		&lt;li&gt;
			This is a 5-day (45hr) learning event (classroom).&lt;/li&gt;
		&lt;li&gt;
			Start/Finish Times: 08:00am – 18:00pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
		&lt;li&gt;
			Prior Learning Requirement: Learners are required to be familiar with ISO 13485:2016 Requirements or have completed a recognised QMS Fundamentals course based on ISO 13485:2016 prior to registering for this course.&lt;/li&gt;
	&lt;/ul&gt;
&lt;/div&gt;
&lt;br&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to Auditing&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Terminology, Principles, QMS Audits&lt;/li&gt;
						&lt;li&gt;
							Auditor Code of Ethics&lt;/li&gt;
						&lt;li&gt;
							Management of an Audit Program&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology, Principles, QMS Audits&lt;/li&gt;
						&lt;li&gt;
							Audit Life Cycle (On-site &amp;amp; Off-site Audit Activities)&lt;/li&gt;
						&lt;li&gt;
							Auditor/Auditee Roles, Responsibilities*&lt;/li&gt;
						&lt;li&gt;
							Desired Auditor Behaviours**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to QMS Auditing &lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Process Terminology*&lt;/li&gt;
						&lt;li&gt;
							Process Models/Methodology &amp;amp; Categories*&lt;/li&gt;
						&lt;li&gt;
							Evaluation of the effectiveness of a Process*&lt;/li&gt;
						&lt;li&gt;
							Processes and the application of PDCA and Risk*&lt;/li&gt;
						&lt;li&gt;
							The QMS Certification Cycle &amp;amp; 3rd Party Certification**&lt;/li&gt;
						&lt;li&gt;
							Special Conformity Audits**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Compliance Auditing &amp;amp; Methodology**&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Medical Device Life Cycle &amp;amp; the Regulatory Audit Perspective**&lt;/li&gt;
						&lt;li&gt;
							Overview of Different Regulatory Requirements [EU, U.S, Japan, Canada &amp;amp; More]**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Trails&lt;/li&gt;
						&lt;li&gt;
							Purpose and benefits for establishing initial contact and forms of contact&lt;/li&gt;
						&lt;li&gt;
							Case Study: Document Review&lt;/li&gt;
						&lt;li&gt;
							Audit Plan&lt;/li&gt;
						&lt;li&gt;
							Audit Checklist&lt;/li&gt;
						&lt;li&gt;
							Audit Protocol&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Onsite Activities&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Lead Auditor Leadership and Supervision**&lt;/li&gt;
						&lt;li&gt;
							Responsibilities of the Lead Auditor&lt;/li&gt;
						&lt;li&gt;
							Communication throughout the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Monitoring Audit Progress&lt;/li&gt;
						&lt;li&gt;
							Consensus and Resolution Conflicts&lt;/li&gt;
						&lt;li&gt;
							Lead Auditor Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Reporting&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up&lt;/li&gt;
						&lt;li&gt;
							Auditor/Technical Expert Coaching, Mentoring and Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Collecting and Verifying Information&lt;/li&gt;
						&lt;li&gt;
							Introduction to Audit Findings&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Opening Meeting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Purpose, process and benefit of an Opening Meeting&lt;/li&gt;
						&lt;li&gt;
							Case Study – Opening Meeting&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Reporting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing the Audit Report**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Completing the Audit&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Evaluating Correction &amp;amp; Corrective Action including Root Cause Analysis and Audit Finding Closure&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up Strategies&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting &amp;amp; Role Play&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;span&gt;CQI &amp;amp; IRCA Certified Course (A18242)&lt;/span&gt;&lt;/h4&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;div class=&quot;course_certification_description&quot;&gt;
						&lt;p&gt;&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/CQI-IRCA-Certified-ISO-134852016-Lead-Auditor-Certification-Training-Course-uk.png&quot; style=&quot;width: 250px;&quot;&gt;This course is fully recognized by CQI &amp;amp; IRCA.&lt;/p&gt;
					&lt;/div&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented QMS for Medical Devices&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented QMS [MD] from the unique Kelmac Group® assurance perspective.&lt;/p&gt;
				&lt;p&gt;
					The &lt;strong&gt;Kelmac Group® assurance &lt;/strong&gt;&lt;strong&gt;perspective is unique&lt;/strong&gt; as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at &lt;strong&gt;improving performance of the organization.&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented QMS Case Study [Medical Devices] available in the market and provides the Learner with the mostrealistic practical audit experience available on the market including a ISO 13485 Quality Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; and related documented templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Evaluating Business Processes&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					An important USP of this Kelmac Group course is that we show each Learner how to evaluate &lt;strong&gt;business processes,&lt;/strong&gt; not just ISO processes and align with the strategic intent of the organization. Business Processes include Marketing &amp;amp; Sales, Design Control, Manufacturing, Logistics, Installation, Purchasing, Servicing &amp;amp; HR. We &lt;strong&gt;cover this practically&lt;/strong&gt; and from the QMS [MD] Auditor Perspective.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Live Audit Vs. Facilitated Audit&lt;span&gt;Which is better? Why?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Some competitors offer a “live” audit as part of their training. However a “live audit” of such short duration (&amp;lt;0.5 day typically) is of &lt;strong&gt;limited value&lt;/strong&gt; as the Learner does not get an opportunity to audit an almost fully documented QMS [Medical Devices].&lt;/p&gt;
				&lt;p&gt;
					Kelmac Group’s course includes a “facilitated” audit which enables us to truly &lt;strong&gt;verify the Learner’s core audit skills&lt;/strong&gt; through working with an almost fully documented Quality Management System [Medical Devices].&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;br /&gt;

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	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => ISO 14001:2015 Lead Auditor Training Course | IRCA Certified
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            [cert_name] => EMS Auditor/Lead Auditor based on ISO 14001:2015 Training Course
            [cert_name_line1] => EMS Auditor/Lead Auditor based on
            [cert_name_line2] => ISO 14001:2015 Training Course
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	This &lt;strong&gt;IRCA Certified ISO 14001 Lead Auditor&amp;nbsp;training&lt;/strong&gt; is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete EMS based on ISO 14001:2015 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing [Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a EMS. The facilitated audit of the EMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, audi&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This &lt;strong&gt;IRCA Certified ISO 14001 Lead Auditor&amp;nbsp;training&lt;/strong&gt; is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a complete EMS based on ISO 14001:2015 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing [Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a EMS. The facilitated audit of the EMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques, audi&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	We focus on consistent interpretation &amp;amp; application the requirements of ISO 14001:2015 and the ability to plan, conduct, report and follow up an audit of a&lt;br /&gt;
	different Environmental Management System scenarios to provide Assurance the Environmental Management System meets the needs of the interested parties.&lt;/p&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 5-day (45hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 18:00pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO 14001:2015 Requirements or have completed a recognised EMS Fundamentals course based on ISO 14001:2015 prior to registering for this course.&lt;/li&gt;
&lt;/ul&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Business/Societal Case for ISO 14001:2015&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex SL&lt;/li&gt;
						&lt;li&gt;
							New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							The Relationship between External and Internal Issues, Interested Party Requirements&lt;/li&gt;
						&lt;li&gt;
							Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Leadership&lt;/li&gt;
						&lt;li&gt;
							Effective Communication and Life Cycle Thinking&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to Auditing&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Terminology, Principles, EMS Audits&lt;/li&gt;
						&lt;li&gt;
							Auditor Code of Ethics&lt;/li&gt;
						&lt;li&gt;
							Management of an Audit Program&lt;/li&gt;
						&lt;li&gt;
							Audit Life Cycle (On-site &amp;amp; Off-site Audit Activities)&lt;/li&gt;
						&lt;li&gt;
							Auditor/Auditee Roles, Responsibilities*&lt;/li&gt;
						&lt;li&gt;
							Desired Auditor Behaviours**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to EMS Auditing &lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Aligning the Business Processes and the EMS Model*&lt;/li&gt;
						&lt;li&gt;
							Process Terminology*&lt;/li&gt;
						&lt;li&gt;
							Process Models/Methodology &amp;amp; Categories*&lt;/li&gt;
						&lt;li&gt;
							Evaluation of the Effectiveness of a Process*&lt;/li&gt;
						&lt;li&gt;
							Processes and the Application of PDCA and Risk*&lt;/li&gt;
						&lt;li&gt;
							The EMS Certification Cycle &amp;amp; 3rd Party Certification**&lt;/li&gt;
						&lt;li&gt;
							Special Conformity Audits**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Trails&lt;/li&gt;
						&lt;li&gt;
							Purpose and benefits for establishing initial contact and forms of contact&lt;/li&gt;
						&lt;li&gt;
							Case Study: Document Review&lt;/li&gt;
						&lt;li&gt;
							Audit Plan&lt;/li&gt;
						&lt;li&gt;
							Audit Checklist&lt;/li&gt;
						&lt;li&gt;
							Audit Protocol&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Opening Meeting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Purpose, process and benefit of an Opening Meeting&lt;/li&gt;
						&lt;li&gt;
							Case Study – Opening Meeting&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Onsite Activities&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Lead Auditor Leadership and Supervision**&lt;/li&gt;
						&lt;li&gt;
							Responsibilities of the Lead Auditor&lt;/li&gt;
						&lt;li&gt;
							Communication throughout the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Monitoring Audit Progress&lt;/li&gt;
						&lt;li&gt;
							Consensus and Resolution Conflicts&lt;/li&gt;
						&lt;li&gt;
							Lead Auditor Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Reporting&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up&lt;/li&gt;
						&lt;li&gt;
							Auditor/Technical Expert Coaching, Mentoring and Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Collecting and Verifying Information&lt;/li&gt;
						&lt;li&gt;
							Introduction to Audit Findings&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Reporting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing the Audit Report**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Completing the Audit&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Evaluating Correction &amp;amp; Corrective Action including Root Cause Analysis and Audit Finding Closure&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up Strategies&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting &amp;amp; Role Play&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;span&gt;CQI &amp;amp; IRCA Certified Course (A14128)&lt;/span&gt;&lt;/h4&gt;
				&lt;div class=&quot;course_certification_logo&quot;&gt;
					&lt;p&gt;&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/cqi and irca course.png&quot; style=&quot;width: 250px;&quot;&gt;&lt;br&gt;&lt;/p&gt;
				&lt;/div&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully recognised by CQI &amp;amp; IRCA.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description3] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented EMS&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented EMS from the unique Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&lt;/p&gt;
				&lt;p&gt;
					We boast the most comprehensive documented EMS Case Study available including an Integrated EHS (ISO 14001 &amp;amp; OHSAS 18001/ISO 45001) Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; the organization’s environmental aspects/impacts register, the organization’s statutory and regulatory and other legal obligations register, the organization’s emergency preparedness and response plan and the organization’s risk register, and related documented environmental templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Evaluating Business Processes&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					One of the most important USPs of this Kelmac Group course is that we show each Learner how to evaluate business processes, not just ISO processes and align with the strategic intent of the organization.&lt;/p&gt;
				&lt;p&gt;
					Business Processes include Marketing &amp;amp; Sales, Design, Manufacturing, Logistics, Installation, Purchasing &amp;amp; HR. We cover this practically and from the EMS Auditor Perspective.&lt;/p&gt;
				&lt;p&gt;
					&lt;strong&gt;Others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
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            [name] => Medical Devices Risk Management Overview based on ISO 14971:2012 Training Course
            [title_name] => ISO 14971 Risk Management Requirements Training Course | Kelmac Group Ireland
            [cert_name] => Medical Devices Risk Management Overview based on ISO 14971:2012 Training Course
            [cert_name_line1] => 
            [cert_name_line2] => 
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	This learning event is aimed at those looking to gain a comprehensive understanding of Medical Device Risk Management based on ISO 14971:2012.&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This learning event is aimed at those looking to gain a comprehensive understanding of Medical Device Risk Management based on ISO 14971:2012.&lt;/p&gt;

            [description1] => &lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 2-day (18hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day)&lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

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				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Introduction and Welcome Workshop objectives and program&lt;/li&gt;
						&lt;li&gt;
							Introduction to Quality Risk Management&lt;/li&gt;
						&lt;li&gt;
							ISO 14971:2012 Requirements&lt;/li&gt;
						&lt;li&gt;
							Introduction to ISO 14971 including the differences between ISO 14971:2007; ISO 14971:2009 and ISO 14971:2012; Overview of the Risk Management Process; Responsibilities; and Requirements of ISO 14971:2012 [Risk Assessment and Control]&lt;/li&gt;
						&lt;li&gt;
							ISO 14971:2012 Requirements&lt;/li&gt;
						&lt;li&gt;
							Requirements of ISO 14971:2012 continued [Risk Documentation, Risk Communication and Risk Monitoring and Effectiveness Review]&lt;/li&gt;
						&lt;li&gt;
							Risk Management Methodologies and Tools Risk Management Methodologies; Risk Management Tools and techniques&lt;/li&gt;
                            &lt;li&gt;
							Application of Quality Risk Management Case Study - Impact of ISO 14971 on the Medical Device Organization/Product Life Cycle&lt;/li&gt;
                            &lt;li&gt;
							Discussion and Q+A&lt;/li&gt;
                            &lt;li&gt;
							Summary and Close&lt;/li&gt;&lt;/ul&gt;&lt;/li&gt;&lt;li class=&quot;learning_topic&quot;&gt;&lt;ul&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;/h4&gt;
				&lt;div class=&quot;course_certification_logo&quot;&gt;
					&lt;p&gt;
						&lt;/p&gt;
				&lt;/div&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully certified by Kelmac Group.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
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            [review_coursecat_id] => 
            [name] => ISO 9001:2015 Lead Auditor Certification Training Course | IRCA Certified
            [title_name] => ISO 9001:2015 Lead Auditor Certification Training Course | IRCA | Quality, QMS
            [cert_name] => 
            [cert_name_line1] => QMS Auditor/Lead Auditor based on
            [cert_name_line2] => ISO 9001:2015 Training Course
            [cert_name_line3] => 
            [cat_desc] => &lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;IRCA Certified ISO 9001 Lead Auditor Training Course&lt;/strong&gt;&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a completeQMS based on ISO 9001:2015 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing [Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a QMS. The facilitated audit of the QMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques,&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	This&amp;nbsp;&lt;strong&gt;IRCA Certified ISO 9001 Lead Auditor Training Course&lt;/strong&gt;&amp;nbsp;is based on assisting and verifying the competencies/capabilities of the Learner to be able to effectively audit a completeQMS based on ISO 9001:2015 requirements with specific emphasis of 2nd Party auditing [Customer/Supplier audits] and 3rd Party auditing [Certification Bodies].&lt;/p&gt;
&lt;p&gt;
	During the delivery, the Learner will complete a Consultant facilitated complete systematic audit of a QMS. The facilitated audit of the QMS, will cover the full audit life cycle as defined by ISO 19011 and the Learner will have to demonstrate and be assessed on the effective application of audit tools and techniques,&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;&lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot; /&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	With an &lt;strong&gt;additional 5 hours of learning&lt;/strong&gt; compared to our competitors, we cover new and additional topics in more depth. We focus on auditing that &lt;strong&gt;provides Assurance&lt;/strong&gt; that the Quality Management System meets the needs of the interested parties &amp;amp; our Learners are equipped to make &lt;strong&gt;higher quality insights for improved organizational performance.&lt;/strong&gt;&lt;/p&gt;
&lt;/div&gt;&lt;div class=&quot;six-step&quot;&gt;
&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot; /&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 5-day (45hr) learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 17:30pm (each day) with an earlier finish on the final day at 2pm&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirement: Learners are required to be familiar with ISO 9001:2015 Requirements or have completed a recognised QMS Fundamentals course based on ISO 9001:2015 prior to registering for this course.&lt;/li&gt;
&lt;/ul&gt;&lt;/div&gt;

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	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Business/Societal Case for ISO 9001:2015*&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex SL&lt;/li&gt;
						&lt;li&gt;
							New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							The Relationship between External and Internal Issues, Interested Party Requirements&lt;/li&gt;
						&lt;li&gt;
							Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Leadership&lt;/li&gt;
						&lt;li&gt;
							Effective Communication and Life Cycle Thinking&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to Auditing&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Terminology, Principles, QMS Audits&lt;/li&gt;
						&lt;li&gt;
							Auditor Code of Ethics&lt;/li&gt;
						&lt;li&gt;
							Management of an Audit Program&lt;/li&gt;
						&lt;li&gt;
							Audit Terminology, Principles, QMS Audits&lt;/li&gt;
						&lt;li&gt;
							Audit Life Cycle (On-site &amp;amp; Off-site Audit Activities)&lt;/li&gt;
						&lt;li&gt;
							Auditor/Auditee Roles, Responsibilities*&lt;/li&gt;
						&lt;li&gt;
							Desired Auditor Behaviours**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to QMS Auditing &lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Process Terminology*&lt;/li&gt;
						&lt;li&gt;
							Process Models/Methodology &amp;amp; Categories*&lt;/li&gt;
						&lt;li&gt;
							Evaluation of the effectiveness of a Process*&lt;/li&gt;
						&lt;li&gt;
							Processes and the application of PDCA &amp;amp; Risk*&lt;/li&gt;
						&lt;li&gt;
							The QMS Certification Cycle &amp;amp; 3rd Party Certification**&lt;/li&gt;
						&lt;li&gt;
							Special Conformity Audits**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Trails&lt;/li&gt;
						&lt;li&gt;
							Purpose and benefits for establishing initial contact and forms of contact&lt;/li&gt;
						&lt;li&gt;
							Case Study: Document Review&lt;/li&gt;
						&lt;li&gt;
							Audit Plan&lt;/li&gt;
						&lt;li&gt;
							Audit Checklist&lt;/li&gt;
						&lt;li&gt;
							Audit Protocol&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Opening Meeting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Purpose, process and benefit of an Opening Meeting&lt;/li&gt;
						&lt;li&gt;
							Case Study – Opening Meeting&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Onsite Activities&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Lead Auditor Leadership and Supervision**&lt;/li&gt;
						&lt;li&gt;
							Responsibilities of the Lead Auditor&lt;/li&gt;
						&lt;li&gt;
							Communication throughout the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Monitoring Audit Progress&lt;/li&gt;
						&lt;li&gt;
							Consensus and Resolution Conflicts&lt;/li&gt;
						&lt;li&gt;
							Lead Auditor Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Reporting&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up&lt;/li&gt;
						&lt;li&gt;
							Auditor/Technical Expert Coaching, Mentoring and Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Collecting and Verifying Information&lt;/li&gt;
						&lt;li&gt;
							Introduction to Audit Findings&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Reporting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing the Audit Report**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Completing the Audit&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Evaluating Correction &amp;amp; Corrective Action including Root Cause Analysis and Audit Finding Closure&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up Strategies&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting &amp;amp; Role Play&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;span&gt;CQI &amp;amp; IRCA Certified Course (A18114)&lt;/span&gt;&lt;/h4&gt;
				&lt;div class=&quot;course_certification_logo&quot;&gt;
					&lt;p&gt;
						&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/cqi and irca course.png&quot; style=&quot;width: 250px;&quot;&gt;&lt;/p&gt;
				&lt;/div&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully recognised by CQI &amp;amp; IRCA.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;

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	&lt;div class=&quot;container clearfix&quot;&gt;
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			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented QMS&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented QMS from the &lt;strong&gt;unique&lt;/strong&gt; Kelmac Group® assurance perspective. The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions &lt;strong&gt;aimed at improving performance of the organization&lt;/strong&gt;.&lt;/p&gt;
				&lt;p&gt;
					We boast the &lt;strong&gt;most comprehensive documented QMS Case Study available&lt;/strong&gt; in the market and provides the Learner with the most realistic practical audit experience available on the market including a ISO 9001:2015 Quality Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; and related documented templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Evaluating Business Processes&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					One of the most important USPs of this Kelmac Group course is that we show each Learner how to evaluate &lt;strong&gt;business processes&lt;/strong&gt;, not just ISO processes and align with the strategic intent of the organization. Business Processes include Marketing &amp;amp; Sales, Design, Manufacturing, Logistics, Installation, Purchasing &amp;amp; HR. We &lt;strong&gt;cover this practically&lt;/strong&gt; and from the QMS Auditor Perspective.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					Live Audit Vs. Facilitated Audit&lt;span&gt;Which is better? Why?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Some competitors offer a “live” audit as part of their training. However a “live audit” of such short duration (&amp;gt;0.5 day typically) is of limited value as the Learner does not get an opportunity to audit an almost fully documented QMS.&lt;/p&gt;
				&lt;p&gt;
					Kelmac Group’s course includes a “facilitated” audit which enables us to truly verify the Learner’s core audit skills through working with an almost fully documented Quality Management System.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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            [name] => Combined ISO 14001 and OHSAS 18001 Lead Auditor Training Course | IRCA Certified 
            [title_name] => Combined ISO 14001 and OHSAS 18001 Lead Auditor Training Course | IRCA Certified 
            [cert_name] => 
            [cert_name_line1] => Combined EMS and OHSMS Auditor/Lead
            [cert_name_line2] => Auditor based on ISO 14001:2015
            [cert_name_line3] => &amp; OHSAS 18001:2007 Training Course
            [cat_desc] => &lt;p&gt;
	Our &lt;strong&gt;IRCA Certified Combined ISO 14001 and OHSAS 18001 Lead Auditor training&lt;/strong&gt; teaches Learners the principles, processes, and techniques used for the assessment of and management of Environmental aspects and impacts, Occupational hazards, risk and controls; and, their significance for EMS and OHSMS lead auditors.&lt;/p&gt;
&lt;p&gt;
	This course is the first of its kind integrating two ISO 14001 and OHSAS 18001 lead auditor classes into a single 6-day learning event versus attending two separate 5-day lead auditor classes (for ISO 14001 &amp;amp; OHSAS 18001 separately).&lt;/p&gt;

            [description] => &lt;h4&gt;
	&lt;img src=&quot;/images/course.jpg&quot; style=&quot;width: auto&quot;&gt; Course Overview &lt;span&gt;Who is this course for?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	Our &lt;strong&gt;IRCA Certified Combined ISO 14001 and OHSAS 18001 Lead Auditor training&lt;/strong&gt; teaches Learners the principles, processes, and techniques used for the assessment of and management of Environmental aspects and impacts, Occupational hazards, risk and controls; and, their significance for EMS and OHSMS lead auditors.&lt;/p&gt;
&lt;p&gt;
	This course is the first of its kind integrating two ISO 14001 and OHSAS 18001 lead auditor classes into a single 6-day learning event versus attending two separate 5-day lead auditor classes (for ISO 14001 &amp;amp; OHSAS 18001 separately).&lt;/p&gt;

            [description1] => &lt;div class=&quot;six-step&quot;&gt;&lt;h4&gt;
	&lt;img src=&quot;/images/key-course.jpg&quot; style=&quot;width: auto&quot;&gt; Key Course Learning Outcome &lt;span&gt;Why this course is unique?&lt;/span&gt;&lt;/h4&gt;
&lt;p&gt;
	We focus on consistent interpretation &amp;amp; application the requirements of ISO 14001 &amp;amp; OHSAS 18001 and the ability to plan, conduct, report and follow up an audit of different EH&amp;amp;S Management. System scenarios to provide Assurance the relevant Management System meets the needs of the interested parties.&lt;/p&gt;
&lt;/div&gt;
&lt;div class=&quot;six-step&quot;&gt;&lt;h4&gt;
	&lt;img src=&quot;/images/course-basics.jpg&quot; style=&quot;width: auto&quot;&gt; Course Basics &lt;span&gt;What is essential to know?&lt;/span&gt;&lt;/h4&gt;
&lt;ul&gt;
	&lt;li&gt;
		This is a 6-day learning event.&lt;/li&gt;
	&lt;li&gt;
		Start/Finish Times: 08:00am – 18:00pm (each day).&lt;/li&gt;
	&lt;li&gt;
		Prior Learning Requirements: Learners are required to be familiar with ISO 14001:2015 &amp;amp; OHSAS 18001:2007 Requirements in advance of registering for this training. There are also additional pre-requisites, see our website to review these important details.&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;

            [description2] => &lt;div class=&quot;row gray-bg&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;course-learning clearfix&quot;&gt;
			&lt;div class=&quot;course-learning-title&quot;&gt;
				&lt;img src=&quot;/images/accrediation.jpg&quot;&gt; Course Learning Topics&lt;span&gt;What does the course cover?&lt;/span&gt;&lt;/div&gt;
			&lt;ul class=&quot;clearfix&quot;&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Course Introduction&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							The Business/Societal Case for ISO 14001:2015 &amp;amp; OHSAS 18001:2007&lt;/li&gt;
						&lt;li&gt;
							Purpose and Impact of Annex SL&lt;/li&gt;
						&lt;li&gt;
							New and Revised Terminology&lt;/li&gt;
						&lt;li&gt;
							The Relationship between External and Internal Issues, Interested Party Requirements&lt;/li&gt;
						&lt;li&gt;
							Risks and Opportunities&lt;/li&gt;
						&lt;li&gt;
							Leadership&lt;/li&gt;
						&lt;li&gt;
							Effective Communication and Life Cycle Thinking&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to Auditing&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Terminology, Principles, IMS Audits&lt;/li&gt;
						&lt;li&gt;
							Auditor Code of Ethics&lt;/li&gt;
						&lt;li&gt;
							Management of an Audit Program&lt;/li&gt;
						&lt;li&gt;
							Audit Life Cycle (On-site &amp;amp; Off-site Audit Activities)&lt;/li&gt;
						&lt;li&gt;
							Auditor/Auditee Roles, Responsibilities*&lt;/li&gt;
						&lt;li&gt;
							Desired Auditor Behaviours**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Introduction to IMS Auditing &lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Aligning the Business Processes and the IMS Model*&lt;/li&gt;
						&lt;li&gt;
							Process Terminology*&lt;/li&gt;
						&lt;li&gt;
							Process Models/Methodology &amp;amp; Categories*&lt;/li&gt;
						&lt;li&gt;
							Evaluation of the Effectiveness of a Process*&lt;/li&gt;
						&lt;li&gt;
							Processes and the Application of PDCA and Risk*&lt;/li&gt;
						&lt;li&gt;
							The IMS Certification Cycle &amp;amp; 3rd Party Certification**&lt;/li&gt;
						&lt;li&gt;
							Special Conformity Audits**&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Planning&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Initiating &amp;amp; Preparing for the Audit&lt;/li&gt;
						&lt;li&gt;
							Audit Trails&lt;/li&gt;
						&lt;li&gt;
							Purpose and benefits for establishing initial contact and forms of contact&lt;/li&gt;
						&lt;li&gt;
							Case Study: Document Review&lt;/li&gt;
						&lt;li&gt;
							Audit Plan&lt;/li&gt;
						&lt;li&gt;
							Audit Checklist&lt;/li&gt;
						&lt;li&gt;
							Audit Protocol&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Opening Meeting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Purpose, process and benefit of an Opening Meeting&lt;/li&gt;
						&lt;li&gt;
							Case Study – Opening Meeting&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Onsite Activities&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Lead Auditor Leadership and Supervision**&lt;/li&gt;
						&lt;li&gt;
							Responsibilities of the Lead Auditor&lt;/li&gt;
						&lt;li&gt;
							Communication throughout the Audit Life Cycle&lt;/li&gt;
						&lt;li&gt;
							Monitoring Audit Progress&lt;/li&gt;
						&lt;li&gt;
							Consensus and Resolution Conflicts&lt;/li&gt;
						&lt;li&gt;
							Lead Auditor Leadership&lt;/li&gt;
						&lt;li&gt;
							Audit Reporting&lt;/li&gt;
						&lt;li&gt;
							Audit Follow-Up&lt;/li&gt;
						&lt;li&gt;
							Auditor/Technical Expert Coaching, Mentoring and Evaluation**&lt;/li&gt;
						&lt;li&gt;
							Collecting and Verifying Information&lt;/li&gt;
						&lt;li&gt;
							Introduction to Audit Findings&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
				&lt;li class=&quot;learning_topic&quot;&gt;
					&lt;p&gt;
						&lt;strong&gt;Audit Reporting&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing Audit Findings&lt;/li&gt;
						&lt;li&gt;
							Case Study: Writing the Audit Report**&lt;/li&gt;
					&lt;/ul&gt;
					&lt;p&gt;
						&lt;strong&gt;Completing the Audit&lt;/strong&gt;&lt;/p&gt;
					&lt;ul&gt;
						&lt;li&gt;
							Evaluating Correction &amp;amp; Corrective Action including Root Cause Analysis and Audit Finding Closure&lt;/li&gt;
						&lt;li&gt;
							Audit Follow Up Strategies&lt;/li&gt;
						&lt;li&gt;
							Final Audit Team Meeting&lt;/li&gt;
						&lt;li&gt;
							Closing/Exit Meeting &amp;amp; Role Play&lt;/li&gt;
					&lt;/ul&gt;
				&lt;/li&gt;
			&lt;/ul&gt;
			&lt;div class=&quot;course_certification_terms&quot;&gt;
				&lt;p&gt;
					&lt;em&gt;*Kelmac Group cover this topic in more depth compared to our competitors.&lt;/em&gt;&lt;br&gt;
					&lt;em&gt;**Kelmac Group proven added value as this material is not covered by the IRCA specification or our competitors.&lt;/em&gt;&lt;/p&gt;
			&lt;/div&gt;
			&lt;div class=&quot;course_certification&quot;&gt;
				&lt;img class=&quot;img_left&quot; src=&quot;/images/certificate-icon.jpg&quot;&gt;
				&lt;h4&gt;
					Course Certification&lt;span&gt;CQI &amp;amp; IRCA Certified Course (A17613)&lt;/span&gt;&lt;/h4&gt;
				&lt;div class=&quot;course_certification_logo&quot;&gt;
					&lt;p&gt;
						&lt;img src=&quot;https://www.kelmacgroup.com/image/data/cqi and irca/cqi and irca course.png&quot; style=&quot;width: 250px;&quot;&gt;&lt;/p&gt;
				&lt;/div&gt;
				&lt;div class=&quot;course_certification_description&quot;&gt;
					&lt;p&gt;
						This course is fully recognised by CQI &amp;amp; IRCA.&lt;/p&gt;
				&lt;/div&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;our-cource clearfix&quot;&gt;
			&lt;div class=&quot;our-cource-title&quot;&gt;
				&lt;img src=&quot;/images/effectiveness.png&quot; /&gt; Our Course vs. Our Competitors&lt;span&gt;Why is our course the best? Just some examples explained of how our course goes further&lt;/span&gt;&lt;/div&gt;
			&lt;div class=&quot;clearfix&quot;&gt;
				&lt;h4&gt;
					Working with a Case Study: Almost Full Documented EH&amp;amp;S Management System&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					Each Learner will audit the almost full documented Integrated EH&amp;amp;S Management System from the unique Kelmac Group® assurance perspective.&lt;/p&gt;
				&lt;p&gt;
					The Kelmac Group® assurance perspective is unique as we audit like many professional financial audit practices where the focus is on providing top management with the quality of insight to make decisions and actions aimed at improving performance of the organization.&lt;/p&gt;
				&lt;p&gt;
					Our almost fully documented EH&amp;amp;S includes an Integrated ISO 14001:2015/OHSAS 18001/ISO 45001 Policy Manual; 13 SIPOC processes [Value chain, Support and Management]; 19 procedures; the organization’s environmental aspects/impacts register, the organization’s OHS hazard, risk and controls register, the organization’s statutory and regulatory and other legal obligations register, the organization’s emergency preparedness and response plan and the organization’s risk register, and related documented environmental templates and records.&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;h4&gt;
					One System Model&lt;span&gt;Why is this important?&lt;/span&gt;&lt;/h4&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
				&lt;p&gt;
					The one system model is based on utilizing Business Process Management to enhance ISO based Management Systems and we show the Learner how to evaluate alignment of the business and the EH&amp;amp;S, the environmental aspects/impacts, the OHS hazards, risks and controls and significance business processes [not ISO processes] and align with the strategic intent of the organization.&lt;/p&gt;
				&lt;p&gt;
					&lt;strong&gt;Others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
				&lt;p&gt;
					&amp;nbsp;&lt;/p&gt;
			&lt;/div&gt;
		&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

            [description4] => &lt;div class=&quot;row&quot;&gt;
	&lt;div class=&quot;container clearfix&quot;&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;h1 class=&quot;heading&quot;&gt;
				The Ultimate Business Training Experience&lt;/h1&gt;
			&lt;p&gt;
				The Kelmac Group® has developed a unique tradition of creating learning services that shape the future of conformity and compliance learning solutions for Executive Management, Practitioners and Auditors. &lt;strong&gt;Where others train followers, we train leaders™&lt;/strong&gt;&lt;/p&gt;
		&lt;/div&gt;
		&lt;div class=&quot;six-step&quot;&gt;
			&lt;iframe allowfullscreen=&quot;&quot; frameborder=&quot;0&quot; height=&quot;222&quot; mozallowfullscreen=&quot;&quot; src=&quot;https://player.vimeo.com/video/143114881&quot; webkitallowfullscreen=&quot;&quot; &gt;&lt;/iframe&gt;&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;

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	The focus of the Kelmac Group®&nbsp;QMS Fundamentals based on ISO 13485:2016&nbsp;is to comprehensively introduce Learners to Quality Management System...</p>
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          <a href="iso14001_training"><h3>ISO 14001:2015 Training (Environmental Management)</h3></a>
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          <a href="iso-27001-training"><h3>ISO/IEC 27001:2013 Training (Information Security)</h3></a>
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