dimecres, 6 de maig del 2015

US FDA's GUDID now publicly accessible

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

Medical device market regulators in the US have launched a new website to provide public access to their Global Unique Device Identification Database (GUDID) designed to store device labelers' information about their products.

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