MDR with Brexit: How the Combination is Impacting the European Medical Device Industry

With the COVID-19 crisis, the Medical Device Regulations (MDR) have been pushed back one year, this delay has given a respite for those companies that were not quite ready for the increase regulations.

This delay put the new MDR requirements in the same time period as the impact of Brexit.

In this presentation we will be discussing the status of the medical device industry regarding MDR and Brexit, and what are others doing to get ready.

Attendees will learn:

• What additional requirements are in the MDR?
• How Brexit is impacting submissions to the UK?
• Where is the industry currently at and how many companies feel ready for their first submission?
• What have we learned from the first submissions under MDR?
• What are others doing now, to save time and money?

Presenter: Thor Rollins, Director, Toxicology and E&L Consulting