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Commission facility to monitor CEE (Central and Eastern Europe) directive transpositions..

This article was originally published in Clinica

Executive Summary

Progress on the transposition of the medical devices directives in the 10 countries due to become members of the EU in May 2004 can now be quickly checked and monitored. This is thanks to a feature contained in a new website constructed by Directorate General Enterprise (DGE), the European Commission service responsible for the regulation of medical devices.

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