Marketing surveillance shaping up pre-Review with Dutch Minister feedback to Dalli Action Plan

Interesting developments after the joint plan for action that Commissioner Dalli sent to the member states in the beginning of February this year urging them to step up market surveillance in order to safeguard the credibility of the EU medical devices vigilance system (which are conveniently summarised in his speech of 9 Febuary 2012): the Dutch minister of Health sent a public reply to the European Commission detailing what the Dutch government thinks should be done to make the system more effective and [...] « Read the rest of this article on medicaldeviceslegal »