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