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:
Toolkits/Methodology
Case Studies
WORK GROUP TITLE:
UDI Capture Work Group
CASE STUDY PARTICIPANTS:
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.
White Papers
This case study provides a review of Grady Health System’s transformation from traditional Value Analysis Joint Product Review Team structure to Va