EU MDR and IVDR implementations still on track

By Ronald Boumans, Emergo Group

The European Commission reports that implementation efforts for the EU Medical Devices Regulation (MDR) 2017/45 and In Vitro Diagnostic Medical Devices Regulation (IVDR) 2017/746 remain on track, as well as related efforts regarding Notified Body designations and Eudamed database development.

Get the full story here at the Emergo Group’s blog.

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