by clarvin | Jan 19, 2022 | White Paper
Curious to find out about clinical evidence for medical device software under the new EU regulations?Look no further than our brand new white paper. This is the fourth white paper in a series published by Clarvin, Morris Law, Kickfile, and Devicia. And for the...
by hemsida365 | Mar 21, 2021 | White Paper
The medical device industry is significantly impacted by Brexit, primarily due to the change in the legal landscape. Notably, the departure by Great Britain from the EU medical device regulatory framework leads to the following: • Product registration with...
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