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    • Webinar
      Medical Devices

    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.

    Post market clinical follow up under MDR

    • 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.

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    Richard Holborow, Head of Clinical Compliance, BSI
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