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Revised medtech regulations take effect in the EEA

This article was originally published in Clinica

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Executive Summary

All member states within the European Economic Area should by now have transposed now the EU’s Directive 2007/47/EC, which revises the EU Medical Devices Directive and the AIMD Directive. The date by which it should have taken effect in national laws is December 21 2008.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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