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European Parliament And Council Of EU "Not Far Apart" On Scrutiny Of High-Risk Devices, IVDs

This article was originally published in SRA

Executive Summary

The provision relating to the scrutiny of high-risk products under the proposed EU regulations on medical devices and IVDs has at last made it onto the agenda of the joint talks between the European Parliament, Council of the European Union and the European Commission which were held on December 3.

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