FDA launches new features for AccessGUIDID. The Food and Drug Administration (FDA), in partnership with the National Library of Medicine, on October 19 announced the launch of two new features on AccessGUDID, the public portal to data submitted to the FDA’s Global Unique Device Identification Database (GUDID).
Two new APIs (application program interface) and a download are now available:
These new features are available in beta release for user testing before their full release.
http://accessgudid.nlm.nih.gov/