Co-hosted with TÜV SÜD and Eclevar MedTech
Post-Market Clinical Follow-up (PMCF) requirements under the EU MDR continue to challenge medical device manufacturers with evolving expectations and rigorous evidence demands.
Register now for our upcoming 60-minute live webinar in which PMCF/MDR Lead from Purdie Pascoe, Marcus Torr, will be joined by Dr. Ulrich Nitsche Global Director Clinical Centre of Excellence from TÜV SÜD and Dr. Nikhil A. Khadabadi from Eclevar MedTech.
These leading experts will unpack critical PMCF strategies, share real-world survey experiences, and offer insights on bridging data gaps to achieve regulatory success.
Key takeaways
PMCF from a Notified Body’s Perspective: Understand Notified Body requirements, common pitfalls, and what auditors look for in PMCF planning.
PMCF Surveys: Best Practices & Compliance: Learn the nuts and bolts of designing robust PMCF surveys, collecting high-quality data, and effectively reporting outcomes that align with MDR expectations.
Strategic MDR Submissions: Discover how to integrate PMCF findings into broader clinical evidence packages and streamline the regulatory pathway.
Avoiding Common Pitfalls: Get first-hand insights on how to circumvent frequent PMCF missteps and ensure your data meets regulatory scrutiny.
Why attend?
Stay ahead of EU MDR requirements and learn directly from a seasoned Notified Body expert.
Gain actionable insights to design and execute PMCF surveys that meet regulatory scrutiny.
Learn how to integrate PMCF findings into your clinical and regulatory strategy for seamless MDR submissions.
Network (virtually) with peers and industry thought leaders and get your PMCF questions answered live.
Ready to strengthen your PMCF strategy? Don’t miss this opportunity to gain insider insights from three industry experts. Secure your spot now to learn how to optimize your PMCF approach and navigate the EU MDR with confidence.
Purdie Pascoe PMCF survey expertise
Purdie Pascoe has developed a best-practice approach, approved by EU regulators and compliant with ISO requirements and GDPR regulations, for PMCF surveys. We can support you with the design, implementation, data collection and reporting of your PMCF surveys to ensure you collect appropriate PMCF data to be used within your MDR submissions.