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 medical transcription services request for proposal.
Letter/Comment
On November 21, 2013, AHRMM submitted electronically
Advisory
The FDA UDI ruling has finally arrived - the proposed rule has published.