Suggested region and language based on your location

    Your current region and language

    Workers inspecting product in pharmaceutical factory
    • 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.

    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?

    Contact Us

    Let's shape your organization's future together - BSI Akamai Changes

    Reach out and see how we can help guide you on your path to sustainable operational success.

    Get in touch