Time Right For MDR/IVDR Completion: Devices Guru Predicts Success – But With Possible Casualties
This article was originally published in Clinica
Executive Summary
Gert Bos, executive director and partner at Qserve Group, says that talks on the European Commission’s original September 2012 proposals for a new EU Medical Device Regulation and IVD Regulation have progressed far enough and it is now time to adopt new rules.