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Zdrowie i gospodarka · 27/06/2014

FDA Releases Final Guidance for Global Unique Device Identification Database

The Food and Drug Administration (FDA) has finalized a guidance document for industry and FDA staff on the Global Unique Device Identification Database (GUDID), which outlines the procedures for device labelers to interface with the database, establish accounts, and submit initial devices information.

Source: Federal Register — Food and Drug AdministrationOpen original release →