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Commission proposes stricter rules for some in vitro diagnostics (IVD)

This article was originally published in Clinica

Executive Summary

The European Commission is prepared to modify the draft directive for in vitro diagnostics (IVDs) to increase the proportion of products subject to third-party review, reports Amanda Maxwell. Norbert Anselmann, head of the medical devices sector within the European Commission's directorate for Industrial Policy made the announcement at the Sixth Global Medical Devices Conference in Lisbon.

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