European Commission Sheds Light On MDR/IVDR Progress In Vital Update

A new "rolling plan" provides deadlines for implementing actions, and other efforts, that are necessary to get the new EU Medical Device and IVD Regulations off the ground.

EU Brussels

The industry and other stakeholders finally have some deadlines from the European Commission on when fundamental aspects underpinning the new Medical Device and IVD Regulations should be ready.

The European Commission has published a "rolling plan" for the MDR and IVDR implementation measures; the first half lists out deadlines for 12 implementing acts that are most needed...

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