Medical Devices Training Modules

Medical Devices follow a very different regulatory pathway, with classification and defining the mode of action key to unlocking the route.

Medical Device training modules include:

 

International Regulatory Framework DEV01
Development Pathway for a New Device DEV02
Classification and Rules - EU DEV03
Classification - US DEV04
Borderline - Devices vs Medicines DEV05
GHTF and STED DEV06
Clinical Trials of Devices DEV07
Notified Body Auditing DEV08
Device Labelling DEV09
Post Approval Obligations DEV10

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