Global Unique Device Identification Database (GUDID) Draft Guidance for Industry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

Advisory
Guidance on Humidity Levels in the Operating Room
Guidance on Humidity Levels in the Operating Room
Toolkits/Methodology
Critical Infrastructure Security & Resilience Month 2013 Toolkit
November is Critical Infrastructure Security and Resilience Month.
Guides and Reports
Supply Chain Services Professional's Role in Achieving the Institute of Medicine's Six Aims for Improvement
In 2001 the Institute of Medicine (IOM) published
Letter/Comment
IRS Issues Final Rule Implementing Medical Device Excise Tax
An announcement of the Final Rule issued by the IRS.
Guides and Reports
Report Demonstrates Hospitals Value Group Purchasing Organizations
 
Magazine & Journal Articles
A Broader Focus for Tomorrow's MMs
AHRMM's Cost, Quality, and Outcomes (CQO) Movement will provide training and education to help supply chain professionals make the correlation…