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 has released final guidance on how manufacturers of reusable medical devices should validate instructions for these products.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1EA72zf
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