PMCF Under the MDR | Notified Body Insights, Survey Best Practices, and Strategic Implementation
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.
Watch this complimentary webcast in which PMCF Manager from Purdie Pascoe, Chris Webb, presented with Dr. Ulrich Nitsche Global Director Clinical Centre of Excellence from TÜV SÜD and Dr. Nikhil A. Khadabadi from Eclevar MedTech.
These leading experts unpack critical PMCF strategies, share real-world survey experiences, and offer insights on bridging data gaps to achieve regulatory success.
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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.