No transition period after March 2010, European Commission reiterates
This article was originally published in RAJ Devices
Executive Summary
The European Commission has clarified a number of points relating to how Directive 2007/47/EC – the directive that amends the active implantable medical devices directive (Directive 90/385/EEC) and the medical devices directive (Directive 93/42/EEC) – should be implemented in an effort to “guide a uniform practice throughout the EU”1.