Veeva Systems, the developer of a suite of applications designed for life sciences companies, sees the forthcoming EU Medical Device Regulation (MDR) as an opportunity to strengthen its links with the medtech industry.
The MDR has caused turbulence across the medtech sector, as companies grapple with its stricter requirements and a race against the clock. Frustration has also risen due to delays in designation of notified bodies. The new regulation, 2017/745, will be enforced in full from 26 May 2020
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