EU MDD (Medical Devices Directive) review takes another small step forward
This article was originally published in Clinica
Executive Summary
The review of the EU Medical Devices Directive (MDD) was the main item on the agenda at the European Commission's Medical Device Experts Group meeting on October 19-20, where members of the European Commission's Clinical Evaluation Task Force (CETF) and the Software Task Force tabled their proposed amendments to the Directive for the first time.