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News and Views March 2017

New Medical Device Regulation (MDR) in Europe
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8. Medical Device Networking Meeting
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New Medical Device Regulation (MDR) in Europe

The New European Medical Device Regulation for 2017 

In 2016 the European Parliament, the Council and the Commission came to an agreement on the new medical devices regulation (MDR) and on the In Vitro medical devices regulation (IVDR).  It is to be expected to enter into force in the first part of 2017. 
It is important to know the new specific requirements for your products and the timelines available to make sure that your products and your company is ready for the “New CE” mark.