This one-day course will help you better understand the following:
- EU Medical Device Regulation
- UK & Northern Ireland transitional requirements and timings regarding Brexit
- How to classify your medical device
- Gain useful insights into technical documentation and labelling
- Gain useful insights into clinical evaluation, usability, and what really matters
- Gain lots of insights into helpful guidance, and white papers
Plus, you will be able to ask ‘that question’ to one of the UK’s most experienced medical device consultants.
Click here for more information and to register
*EARLY BIRD OFFER – Book before 5 pm on Tuesday 8th June 2021 (please note this offer does not apply to virtual attendance)