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    • Webinar
      Medical Devices

    Active Implantable Medical Devices under the EU MDR at MedTech Summit 2021

    This webinar discusses technical documentation requirements under the EU Medical Device Regulation.

    Watch the Webinar

    In this webinar:

    • Active Implantable Medical Devices at BSI.

    • Technical documentation requirements under the EU Medical Device Regulation.

    • Obstacles for BSI as a Notified Body.

    • Evidence to support active implantable medical devices when submitting documents for application.

    Active Implantable Medical Devices under the EU MDR at MedTech Summit 2021

    Focusing on software design and clinical evidence to support active implantable medical devices when submitting documents for an MDR application.

    Thomas Doerge, Global Head Active Implantable Medical Devices, BSI
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