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Eucomed: proposed overhaul of EU reg system mostly positive with one caveat

This article was originally published in Clinica

Executive Summary

With Eucomed's annual MedTech Forum underway in Brussels this week, the European medtech trade association's director of regulatory and technical affairs John Brennan gives the industry view on what is undoubtedly the hottest discussion topic among delegates at the forum: the European Commission's proposed revision of the EU medical device directives

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