On Wednesday 21 February, the Committee of Permanent Representatives of the Member States to the EU (Coreper) confirmed the European Parliament/Council agreement on the proposal to give companies more time to implement the regulation on in vitro diagnostic medical devices, subject to certain conditions (see EUROPE B13334A5).
The Regulation amends the legislation on medical devices, including in vitro diagnostic (IVD) medical devices, in the following ways: - by extending the transition...