The new EU MDR is a legal framework that includes three directives designed to regulate the safety of medical devices in Europe. These new regulations are far more comprehensive than previous regulations as the definition of a medical device now widely extends beyond what was considered a medical device in the past.
To get prepared and build safe, effective products that comply with these changing, more stringent MDR regulations, you’ll want to make sure your team is up to speed.
Download this eBook to learn:
- What you need to know about the key MDR changes
- The benefits of regulation revamping
- How to implement the changes and achieve compliance with greater efficiency