Webinar
Medical Devices

Rollout of EU Reference Laboratories for IVDR Class D devices

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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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