New EU device regulation rapporteur causes Commission stir over devices
This article was originally published in Clinica
Executive Summary
Glenis Willmott, the newly-appointed EU Parliament rapporteur for the medical devices regulatory file, has been mobilizing fellow MEPs in the Social & Democrat party into action over the EU Commission’s decision to transfer responsibility of medtech from the health directorate (DG Sanco) to the industry directorate (DG ENTR).
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