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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

    Alex Laan, Head of Notified Body - IVD

    Sara Fabi, Regulatory Lead - IVD
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