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    • Webinar
      Medical Devices

    Understanding the QMS Requirements Under the IVD Regulation

    Rigorous regulatory controls.

    This webinar:

    • Manufacturers of IVD devices selling into Europe.

    • Meeting regulatory requirements and maintaining a Quality Management System (QMS) under IVDR.

    • Support your preparation for an efficient transition or initial certification.

    • Requirements of the Quality Management System.

    Contributors

    For manufacturers of IVD devices selling into Europe

    Key changes for meeting regulatory requirements and maintaining a Quality Management System under the IVDR for transition or initial certification.

    Contributor

    Judith Prevoo

    Regulatory Lead NL, BSI

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