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    • Webinar
      Medical Devices

    Medical Device software under MDR - Perspectives from a Notified Body

    This webinar focuses on Technical Documentation and typical gaps we see as a Notified Body for software applications applying for MDR certification.

    Watch the webinar View the Presentation

    Learn more about Medical Device Regulation requirements for Software

    Including including GSPRs, Applicable guidance, lessons learnt and the interplay between AI and the MDR.

    • MDR requirements for software, GSPRs, guidance and AI interplay.

    • Ideal for start-ups, SMEs and software developers.

    • Key insights on Technical Documentation and common gaps.

    • Lessons from a notified body on MDR certification.

    Speakers

    Hear from these experts in this webinar

    Speaker

    Thomas Doerge

    Global Head AIMD and SaMD

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