The Ins and Outs of Post Market Surveillance Under the EU MDR
Watch this Celegence featured presentation to learn about why the expanded Post Market Surveillance (PMS) requirements are a major hurdle that the EU MDR presents. Notified Bodies will be expecting a far greater amount of Post Market Surveillance data, and device manufacturers must improve their PMS systems and processes to adapt.
In this webinar, you will have an opportunity to learn about:
- The purpose of PMS in the EU MDR
- How to set up an effective PMS system
- How the PMS system should integrate with other systems
- How to keep your PMS system up to date
- Reporting requirements and other PMS obligations of the manufacturer
If you’re curious how Celegence can help improve your Regulatory Operations then contact us now to arrange a meeting!