PMS & PMCF Compliance for Medical Devices Under EU MDR - Webinar 1
Join QbD Group's expert-led webinar series on September 9 and 23 and discover how to turn PMS & PMCF compliance into clinical and strategic advantage — with exclusive insights from a notified body.
Far beyond a compliance checkbox, Post-Market Surveillance (PMS) and Post-Market Clinical Follow-up (PMCF) are essential drivers of product safety, clinical validation, and long-term market success. Through real-world insights and practical strategies, QbD Group will show you how to turn regulatory obligations into strategic advantages.
Register for one or both of our webinars designed to equip you with the knowledge and tools to elevate your PMS and PMCF systems.
- Session 1 | September 9: Navigating Post-Market Compliance Under MDR
Achieving CE marking is just the beginning. This webinar will clarify how Post-Market Surveillance (PMS) and Post-Market Clinical Follow-up (PMCF) requirements shift once your medical device is on the market. You'll get practical guidance on staying compliant under EU MDR—especially for legacy devices already in use.
- Session 2 | September 23: PMCF in Practice – Strategies, Tools & Expert Insights
This session dives into the practical side of PMCF. Our team will share how we approach PMCF activities such as clinical investigations, literature reviews, usability studies, and surveys. A notified body expert will join to provide real audit insights and share what they expect to see in your technical documentation.