Whitepaper
Medical Devices

EU MDR – Post Market Clinical Follow-Up

This whitepaper aims to guide the medical device manufacturer in the implementation of real-world data collection as part of PMCF.

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EU MDR – Post Market Clinical Follow-Up

Download the full whitepaper to understand more about Post-Market Clinical Follow-up (PMCF).

Definitions of PMCF activities under MDR.
Key Changes under MDR.
Analysis of Clinical Data Deficiencies Once.
Real-World Data and PMCF Activities.
What documentation is required for Real-World Evidence in the MDR?
How are Real-World Evidence and Clinical Investigation connected?

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