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  • 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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