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Clinica 100: EMA or JRC – who will manage and oversee EU medtech regulations?

This article was originally published in Clinica

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Executive Summary

One of the clearest indicators of the way EU medtech regulation is heading over the next couple of decades will be revealed in 2012 when the European Commission makes public the future role and location of the forthcoming centralised EU Medical Devices Committee (MDC). Will this body be housed within the European Medicines Agency or the European Commission’s Joint Research Centre? Amanda Maxwell gathers and assesses the different opinions on this critical issue

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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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