It’s never far from our pages, yet one could be forgiven for thinking that European policymakers are still, well, thinking about how to proceed with revisions to the European Medical Devices Directive and its implementation.
Medtech industry body Eucomed’s Director of Regulatory and Technical Affairs, John Brennan, helpfully updates us here with his new blogpost entitled “So where are we again on the Revision of the MDD?”.
It’s a really concise and interesting assessment of the issues and the state of play from the perspective of all stakeholders and teasingly it ends with a promise to discuss the concept of a European PMA, a favourite subject of ours. It also somewhat explains why it’s all taking so long.
Source: Eucomed
published: May 11, 2012 in: Regulatory