Device Week, 3 December 2021 – What Do The New Eudamed Modules Mean For Medtech?
Executive Summary
In this week’s podcast, EU regulatory editor Amanda Maxwell brings listeners up to speed on the latest news from the European Union, including recent module updates and compliance expectations for the Eudamed database.
Listen to the podcast via the player below:
The archive of Device Week and the rest of Informa Pharma Intelligence’s podcasts are available on the Informa Pharma Intelligence channel on Apple Podcasts, Google Podcasts, SoundCloud, TuneIn, Spotify Podcasts and via smart speakers if one of these platforms has been set up as your default podcast provider.
Medtech Insight articles discussing topics addressed in this episode:
-
European Regulatory Roundup, November 2021: Eudamed Dominates News
-
Commission Publishes Implementing Regulation That Acts As Basic Starter Manual For Eudamed
-
Timelines And Deadlines For Stakeholders To Submit Information To EU’s Eudamed Database
-
How Does The Eudamed Module On Notified Bodies And Certificates Work?