Home » Industry Decries ‘Needle in a Haystack’ Approach to Device Scrutiny Proposal
Industry Decries ‘Needle in a Haystack’ Approach to Device Scrutiny Proposal
February 5, 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, industry says in a newly released position paper on proposed revisions to the medical device directives.
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