Training resources
Download individual medical device training course pdfs below.
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UK Medical Devices Training Brochure >
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UK Medical Devices Training Flyer >
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Introduction to CE Marking >
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Medical Device CE Marking >
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Introduction to CE Marking for In Vitro Diagnostics >
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Application of In Vitro Diagnostics Directive >
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ISO 13485:2016 Transition >
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ISO 13485:2016 Auditor Refresher >
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ISO 13485:2016 Transition & Auditor Refresher >
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Introduction to ISO 13485:2016 >
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ISO 13485:2016 Clause by Clause >
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Implementing ISO 13485:2016 >
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Internal Auditor ISO 13485:2016 >
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Lead Auditor ISO 13485:2016 >
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Creating and Maintaining Technical Files and Design Dossiers >
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Introduction to Risk Management for Medical Devices >
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Clinical Evaluation for Medical Devices >
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Post Market Surveillance and Vigilance >
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CE Marking Medical Devices with Software >
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Process Validation for the Medical Device Industry >
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Device-Drug Combinations: Practical Guidance on Borderline Issues and the Consultation Process >
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Medical Devices Utilizing Material of Animal Origin >
