Who’s who at European Commission devices unit: key contacts for your file
This article was originally published in Clinica
Executive Summary
With most people now back at their desks in Brussels after the summer break, and a period of intense medtech regulatory negotiations with the European Commission ahead, the sector will benefit to have some key names at the European Commission’s unit responsible for health technology.
You may also be interested in...
Second EU MDR Notified Body Designated In France
Four years after the designation of the first notified body in France under the Medical Device Regulation, AFNOR Certification has been named too.
EU Regulatory Experts Support Notified Bodies, But Argue For Greater Consistency
Notified bodies have been a pivotal part of the EU medtech regulatory system since it was first launched in the 1990s. Where might they fit within a new medtech regulatory governance structure? Panelists on a recent vodcast grappled with the question.
First Public Discussion On How EU Medtech Regulatory Governance Structure May Evolve
Does the EU need a medtech agency for the first time in its history? Nothing can or should be decided too quickly but five high-profile experts broadly agreed that change is now critical.