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Tag: MDR

Your Questions about the EU MDR, Answered

Posted on February 27th 2020

On January 31, 2020, the United Kingdom left the European Union. And in May of 2020, the European Union will introduce the new EU MDR (Medical Device Regulations), which will modernize the process by which medical devices come to market. So for those who market or manufacture medical devices in the EU, this string of changes might seem confusing. Don’t worry; here, we’ll answer your biggest questions about the new EU MDR.  

Published in MultiPoint Blog

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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