COCIR Contribution to Medical Device Regulation

Since at least 2008, COCIR has been closely monitoring and contributing to the evolution of the new EU Medical Devices Regulation - MDR.  Based on the outcome of the European Parliament’s 22 October 2013 plenary vote, and ongoing discussions with the European Commission and the European Council, we decided to update our January 2013 High Level Contribution.

Read Our updated High Level Contribution on MDR here

In addition, COCIR issued, together with our partner associations – Eucomed, Edma, Eurom VI and Euromcontact – a joint industry position paper on the obligations for economic operators, under the scope of the current MDR.

Read Joint industry Position Paper on economic operators here