Fit for MDR
The new Medical Device Regulation imposes strict demands on medical device manufacturers and the Notified Bodies whom they must involve in the approval process of medical devices other than self-declaration class I devices. While advanced preparation and early action is key to ensuring a smooth transition to the new requirements, medical device manufacturers are expected to encounter challenges pertaining to review and approval processes, among others.
To address these challenges, TÜV SÜD’s experts will share insights on key changes, assessment procedures and other requirements, through our ‘Fit for MDR’ series of complimentary webinars. Know more about out topics and register for the same below:
Part 1 : Biocompatibility
On-demand video available | Watch now
Part 2 : Packaging
On-demand video available | Watch now
Part 3 : Sterilization
On-demand video available | Watch now
Part 4 : TD Assessment
On-demand video available | Watch now