[eBook]Understanding the EU Medical Device Regulation
The new European Union (EU) Medical Device Regulation (MDR) comes into effect on May 26, 2020, replacing the existing EU Medical Devices Directive (MDD). It will bring new products into scope and require many devices to be recertified.
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!