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
Request for Proposals (RFP)
A sample of a bed management RFP covering all the basics. Download the document and tailor it to your needs.
White Papers
This white paper explores the realities facing healthcare delivery, some of the new models being developed and what they could mean for the s
Letter/Comment
AHRMM comments to the FDA regarding an amendment to the UDI proposed rule to address the UDI implementation time frame required by the 2012 Fo