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    Laboratories
    • Webinar
      Medical Devices

    Rollout of EU Reference Laboratories for IVDR Class D devices

    Watch the Webinar View the Presentation

    Key takeaways and learning objectives

    • What is the status of the implementation of the EURLs becoming operational, as of October 1, 2024?

    • What will the EURLs expect to receive from BSI and IVD manufacturers after October 1, 2024?

    • How will the Class D IVD batch verification and performance verification process be monitored?

    • What kind of engagement is expected from IVD manufacturers in relation to the EURLs?

    Speakers

    Presenter information

    Speaker

    Alex Laan

    Head of IVD Notified Body, BSI
    Speaker

    Sara Fabi

    Regulatory Lead, IVDR, BSI
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