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
Canadian medical device market regulator Health Canada will begin requiring all reprocessed single-use medical devices to Canadian Medical Device Regulations (CMDR) by September 1, 2015.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1FUk36O
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