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Does your company manufacture or market medical devices in the European Union? Then you’re probably aware of the upcoming implementation of the EU Medical Device Regulations in May of 2020. And for IVD manufacturers, the new In Vitro Diagnostics Regulation goes into effect May of 2022. But whether you have four months or two years to prepare, you must be educated on the new regulations, which will modernize the processes by which medical devices and IVDs come to market.

Published in MultiPoint Blog

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