Why IP needs a refresh with EU medical devices regulations

24 November 2017

Sheena discusses the new EU regulations governing medical devices (MD) and in vitro diagnostic devices (IVD) which came into effect in May 2017 and whose full application will commence in 2020 and 2022 respectively.

Planning and action should start now to make the most of the opportunities and minimise the threats of the new regulations. One area where new strategies may be needed is Intellectual Property (IP).

Sheena's full article is published on Med-tech Innovation News’s website and can be viewed here. (links to external site)

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