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Home » Industry Criticizes ‘Random’ Approach of EU Device Scrutiny Proposal
Industry Criticizes ‘Random’ Approach of EU Device Scrutiny Proposal
February 8, 2013
The European Commission should replace its “random” premarket control mechanism for high-risk medical devices with a systematic procedure that applies to all Class III devices, Eucomed says in a position paper on proposed revisions to the 2007 medical device directives.