Webinar
Medical Devices

IVDR Regulatory Updates

Where do we stand 18 months after DoA?

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In this Webinar:

A short recap on where the IVDR is (latest MDCG guidance and developments in Brussels).
Description of the challenges for Class D IVD’s and the status on EU Reference Labs.
Envision the potential ramifications for manufacturers of these updates.
IVDR moving forth from here.

Speakers

Hear from the experts in this webinar

Speaker

Alex Laan

Head of IVD Notified Body, BSI

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