[eBook]Understanding the EU Medical Device Regulation
The new European Union Medical Device Regulation (MDR) will replace the EU Medical Devices Directive (MDD), bringing new products into scope. Changes to the EU MDR have seen the deadline amended, requiring many devices to be recertified by May 26, 2021 instead of the original May 26, 2020 deadline.
What’s included in this eBook?
This eBook provides information on implementing the new EU MDR to maintain market access, and certifying in-scope products before the deadline.
The eBook offers insight on:
- How medical devices are classified.
- Processes to gain compliance under the new MDR.
- The difference between the former medical device regulation and the new MDR.
- Best practices for maintaining market access.
- …And more!
Download the eBook now!