Global Unique Device Identification Database (GUDID) Draft Guidance for Industry

By Center for Devices and Radiological Health, Informatics Staff, U.S. Department of Health and Human Services Food and Drug Administration, AHRMM
This document is intended to provide information about submitting data to the database for device Labelers, entities responsible for providing the data to the GUDID.
 

Related Resources

Webcast
GPO or Local/Self Contracting Series: Compliance and Alignment – Part 3
Part 3 of the GPO or Local/Self Contracting webcast series examines whether compliance can be achieved without alignment, and vice versa.
On-Demand Educational Webinars
Cost Savings Through Spend Control: The General Contract Policy
Uncontrolled and unchanneled spend through purchase order requests, P-Card use, or petty cash pose a major problem. In this webinar, we show how to…
Webcast
GPO or Local/Self Contracting Series: Expectations of GPO Partners and Summary – Part 4
Panelists in Part 4 of the GPO or Local/Self Contracting webcast series focus on what providers should expect from their GPO partners. In a Part 5…
On-Demand Educational Webinars
Shared Risk Contracting: Provider and Supplier Perspectives
New risk sharing models align the economics of an agreement to product or service performance and outcomes. In this webinar, we discuss this…
e-Learning
Supply Chain: Owning the Intersection of Cost, Quality, and Outcomes
e-Learning
The Process of Operationalizing Contracts to Support CQO