This course is designed to provide a detailed understanding of the UK regulatory landscape for medical devices or in vitro diagnostic devices, focusing on how to navigate current regulations, prepare for future changes, and develop an effective transition strategy.

The training will also cover essential post-market surveillance requirements to ensure ongoing compliance.

This course will help training participants gain in-depth knowledge about the UK’s evolving regulatory environment and learn how to prepare for upcoming changes, including post-market surveillance requirements and developing a robust transition strategy.