divendres, 4 d’agost del 2017

Chinese regulators answer two common clinical trial questions

Emergo GroupBy Stewart Eisenhart, Emergo Group

China Food and Drug Administration (CFDA) regulators have addressed frequently asked questions regarding clinical trial requirements for medical devices.

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 Chinese regulators answer two common clinical trial questions appeared first on MassDevice.



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