AMDR comments on issues of EU single-use medical devices specifications

AMDR comments on issues of EU single-use medical devices specifications

The Association of Medical Device Reprocessors urged the European Commission to delete provisions of Article 5 of its specifications for reprocessing single-use medical devices because of a lack of legal basis for placing obligations on device makers, and to make various other revisions to the draft implementing act for the specifications…

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By |2019-09-12T18:13:39+00:00August 30th, 2019|In the Press|0 Comments