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.
![](https://www.assent.com/wp-content/uploads/2019/06/Screen-Shot-2022-06-14-at-2.44.50-PM-255x300.png)
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!