The Official Comment of AHRMM to the United States Department of Health and Human Services Food and Drug Administration (FDA) regarding Unique Device Identification for Medical Devices Docket No. FDA-2011-N-0090
AHRMM comments to the FDA regarding an amendment to the UDI proposed rule to address the UDI implementation time frame required by the 2012 Food and Drug Administration Safety and Innovation Act (FDASIA).
Related Resources
Case Studies
WORK GROUP TITLE:
UDI Capture Work Group
CASE STUDY PARTICIPANTS:
Case Studies
A UDI Capture Work Group Case Study at the Beaver Dam Community Hospitals, Inc.
Guides/Reports
As the Institute for Healthcare Improvement’s (I
Case Studies
AHRMM is building a repository for leading and proven supply chain practices, case studies, and toolkits that are developed from a
Issue Brief
This Awareness Brief provides a high level summary understanding of value based purchasing.
Issue Brief
This Awareness Brief provides a quick reference to the