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    Webinar - Claiming equivalence under the MDR regulatory considerations
    • Webinar
      Medical Devices

    Claiming Equivalence Under the MDR – Regulatory Considerations

    Reviewing MDR Requirements, General principles of Equivalence under the MDR and Regulator aspects of Equivalence based on classification.

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    This webinar:

    • General principles of Equivalence under MDR.

    • Regulatory aspects of Equivalence based on classification.

    • Clinical data for Equivalent devices.

    • Similar devices.

    Speakers

    Hear from the experts in this webinar

    Speaker

    Richard Holborow

    Head of Clinical Compliance, BSI
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