10 questions companies affected by European MDR should be asking

By Ronald Boumans and Stewart Eisenhart, Emergo Group

Now that the European Parliament has voted to approve the Medical Device Regulations (MDR), many medical device companies active in Europe have begun mapping out how the new Regulations will impact their business. Based on feedback from clients as well as our own analysis of the MDR, Emergo has identified ten common industry questions and concerns regarding the EU Parliament-approved new regulation.

Get the full story here at the Emergo Group’s blog.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.

The post 10 questions companies affected by European MDR should be asking appeared first on MassDevice.

from MassDevice http://ift.tt/2pwN6ee