divendres, 28 de desembre del 2018

FDA finalizes guidance on Breakthrough Medical Device market pathway

Emergo GroupBy Stewart Eisenhart, Emergo Group

The US Food and Drug Administration has finalized details of a new registration route for breakthrough medical devices first announced in 2017.

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 FDA finalizes guidance on Breakthrough Medical Device market pathway appeared first on MassDevice.



from MassDevice http://bit.ly/2ViyBuS

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