The Emergo Group Blog provides short updates on quality and regulatory topics that may be of interest to QA/RA professionals in the medical device and IVD industry. No fluff, just straight to the point. We hope you'll enjoy the content.
By Stewart Eisenhart, Emergo Group
The US Food and Drug Administration's Center for Devices and Radiological Health (CDRH) has formally launched a new database compiling all guidance documents pertinent to medical device manufacturers with products registered for sale in the US.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1APUNhh
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