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
Malaysia's Medical Device Authority, responsible for overseeing the country's medical device market, has published new draft guidance on post-market surveillance regulatory audits for manufacturers authorized to sell their products there.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1GTllB4
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