divendres, 20 de març del 2015

Final US FDA guidance on instructions and labeling for reprocessed medical devices




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.





Emergo Group

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.




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