Post Market Surveillance under the EU MDR – Challenges and Best Practices

Post Market Surveillance (PMS) under the EU Medical Device Regulation (EU MDR 2017/745) is an area of huge interest to Manufacturers looking to do business in Europe.

On Wednesday, 29th January 2025, Comply Guru’s Michelle Keane discussed the challenges and best practices for Post Market Surveillance (PMS) under the EU Medical Device Regulation (EU MDR 2017/745).

This Webinar will discuss key topics including:

1. Lack of Real-World Data
2. Resource Constraints
3. Use of Digital Tools and Automation
4. Ensuring Cross-Functional Collaboration
5. Auditing Post Market Surveillance

Register for FREE to gain access to this Webinar (On-demand for 30-days). Please note that registration is required to join.