Global Unique Device Identification Database (GUDID) Draft Guidance for Industry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

On-Demand Educational Webinars
Now's the Time! We Must Engage Physicians to Reduce Costs and Improve Outcomes
This AHRMM webinar will help engage physicians to reduce costs and improve patient outcomes.
On-Demand Educational Webinars
Product Disruptions Are Impacting My Business Continuity
Business continuity ensures that an organization can continue to operate in the event of a serious incident or disaster and encompasses strategic…
Webcast
Revenue Cycle Basics: Components and Terminology 101– Part 1
Part 1: Components and Terminology 101 This series of short education sessions documents various aspects of the Revenue Cycle and how it impacts Su
On-Demand Educational Webinars
Cracking the Bullwhip - See How Demand Variation Affects the Supply Chain
Increased demand can lead to reactive replenishment but triggers be identified and assessed before rushing to order. Take control of your inventory…
On-Demand Educational Webinars
Introduction to Benchmarking
In today’s value-based care environment, hospitals continually strive to improve patient quality and outcomes. Benchmarking is a powerful tool that,…
On-Demand Educational Webinars
Managing Supply Chain in Health Care Reform
This webinar discusses the health care supply chain, its strengths and weaknesses. It reviews best practices around the industry, including what…