Global Unique Device Identification Database (GUDID) Draft Guidance for Industry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
Special Fraud Alert: Physician-Owned Entities
This Special Fraud Alert focuses on the specific attributes and practices of PODs that OIG believes produce substantial fraud and abuse risk and pose…
Request for Proposals (RFP)
Transcription Services
A sample of medical transcription services request for proposal.
Request for Proposals (RFP)
Architect RFP
Please see a sample of a Architect RFP below - you will find this short document covers all the basics, and you can tailor it to your needs.<
Request for Proposals (RFP)
General Contractor RFP
A sample of a general contractor RFP.
Request for Proposals (RFP)
Generic Reference Lab RFP
A sample of generic reference lab request for proposal.
Issue Brief
Medical Device Excise Tax - What You Should Know
The Medical Device Excise Tax, a component of the Affordable Care Act, is approaching implementation at the beginning of 2013.