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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.
Discover how to turn PMS & PMCF compliance into clinical and strategic advantage.
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Agenda
00:00 – Introduction
03:50 – PMS after EU market approval
18:30 – PMS versus PMCF
21:44 – Data sources
29:17 – PMCF challenges & solutions
36:22 – Q&A
51:04 – Key takeaways and closing remarks
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Our support
Do you like to know how we can help you with tailored, efficient, and MDR-compliant strategies that turn regulatory obligations into clinical and commercial value? Discover our end-to-end PMCF support, from strategy to execution.
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