The roadmap to EU-MDR Implementation

The availability of the text for the new European Medical Device Regulation (EU-MDR) allows manufacturers to start considering the impact on their activities, and what they will need to do to be compliant with the revised requirements.

This MDR will overhaul some of the basic principles with which you have been working, under the Medical Device Directive (MDD).

Post date: April 01, 2017
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