Upcoming Webinar: Key Considerations for Implementing Post-Market Clinical Follow-Up (PMCF) for Medical Devices
Topic: The European Medical Device Regulation (MDR) and Effective PMCF Strategies
Date: 19 Sep 2024, 3 pm CET
Registration Link: https://www.greenlight.guru/webinar/key-considerations-for-implementing-post-market-clinical-follow-up-for-medical-devices-partner
The European Medical Device Regulation (MDR) introduced the concept of Post-Market Clinical Follow-Up (PMCF) to ensure the continued safety and performance of medical devices after they enter the market. We are excited to contribute to this informative webinar, designed to help medical device manufacturers establish an effective PMCF process.
Specifically, this webinar will cover:
- Key considerations for creating a robust PMCF plan
- Strategies for planning and executing PMCF studies,
- Best practices for using EDC systems in PMCF activities
Who Should Attend:
Medical device manufacturers, regulatory professionals, and quality assurance teams.
