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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.

    Download the Whitepaper

    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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