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
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
Advisory
Executive Summary
Today’s healthcare environment is rapidly changing.
Magazine & Journal Articles
Jim Smoker, CMRP, MPA, CS, York, Pennsylvania
Press Releases
CHICAGO (December 19, 2013) – The Association for Healthcare Resource & Materials Management (AHRMM) of the American Hospital Association poste