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
Now that US medical device regulators have begun implementing their Unique Device Identification (UDI) system, many device manufacturers are questioning how best to comply with the new requirements in the most efficient manner possible. At Emergo, we've identified seven key (and common) issues firms should consider as they undertake their UDI compliance projects.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1HU6OqS
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