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
Clinical Trials of Devices DEV07
Notified Body Auditing DEV08
Device Labelling DEV09
Post Approval Obligations DEV10

Contact Us

T: +44 (0)1276 671 166
F: +44 (0)1276 670 960

Email Us

Find Us

RRG, Innovation House
Albany Park, Camberley
Surrey. GU16 7PL

View Map

Latest News

We have placed cookies on your computer to help make this website better. You can change your cookie settings at any time. Otherwise, we'll assume you're OK to continue.