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:
Presenter: Thor Rollins, Director, Toxicology and E&L Consulting
Want to sponsor? Contact us to find out more.