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    • Webinar
      Medical Devices

    Clinical Masterclass Series 2022 Post Market Clinical Follow Up Under MDR

    The medical device regulations specifically state that post-market clinical follow-up is a continuous process under the regulations.

    Watch the Webinar View the Presentation

    In this Webinar:

    • PMS and PMCF requirements: where are they defined?

    • Does PMCF under the MDR mean the same as PMCF under the directives?

    • Types and plans of PMCF.

    • PMCF Reports.

    Post market clinical follow up under MDR

    BSI interpretation of post market clinical follow up under the MDR.

    Richard Holborow, Head of Clinical Compliance, BSI
    Insights & Media

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    IVDR Companion Diagnostics (CDx) Update - Two biologists in a laboratory
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    IVDR Companion Diagnostics (CDx) Update

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    Clinical Evaluation for Medical Software & AI Devices

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