EU ENVI Parliamentary Committee resolution re Review : “learn the lessons of this fraud” and an FDA internal report

The European Parliament’s ENVI Committee (Committee on the Environment, Public Health and Food Safety) has added to the political pressure on the European Commission that is currently working on the proposal of the Review of the medical devices directives, still scheduled for the end of Q2 2012 as far as I know. At its meeting on 25 April is unanimously passed a resolution requesting the Commission to implement among other things in the words of the press release: A breast implant register, more strin [...] « Read the rest of this article on medicaldeviceslegal »