Transition Periods

Patient problem adverse event codes published

MedTech Europe position on the proposed draft Standardisation Request for In-vitro Diagnostic Medical Devices (IVD) Regulation (2017/746/EU) and Medical Devices (MD) Regulation (2017/745/EU)

Transition Periods

The transition to a new regulatory framework for in vitro diagnostic medical devices in the European Union

European IVD Industry Welcomes Plenary Vote But Remains Concerned with the Three-Year Transition Period

European IVD industry welcomes plenary vote but remains concerned with the three-year transition period

MDD fact sheet: Transition period

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