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EU industry responds to Lalis' letter and latest MDD (Medical Devices Directive) review text

This article was originally published in Clinica

Executive Summary

Eucomed, the European medical technology industry association, is disappointed that many of the issues that it has flagged as priorities in the context of the review of the Medical Devices Directive (MDD) have seemingly not been taken up by the Commission in the latest text of the proposed review. Although this text had still not been published as Clinica went to press, Commission director, Georgette Lalis, who oversees medical device legislation, has recently written a letter to those who responded to the public consultation on the review concerning the outcome of that consultation.

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