UDI and Providers: What You Need to Do
Get the basics on what healthcare supply chain and manufacturers, together with clinical and IT departments, must do to implement the Unique Device Identifier and adverse event reporting, and the subsequent effects that will trickle-down to individual patients and the global health population.
Related Resources
Guides and Reports
Overview:
The Business Case for the UDI work group, a formal work group of the Association for Healthcare Resource & Materials Manage
Webcast
This short webcast will give you a brief overview of the current ISM® Report On Business, share details surrounding the development of the new
Webcast
In this AHRMM webcast, Karen Conway, executive director of industry relations and value at GHX discusses her research with the FDA on the val
Advisory
An announcement of GUDID Release 2.2 deployment and document updates.
Webcast
Susan Morris, CMRP, FAHRMM, health care executive, Cerner Corporation, explains the different parts of the Unique Device Identifier (UDI) and