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
AHRMM is developing a repository for leading and proven supply chain practices, case studies, and toolkits that are developed from a
Request for Proposals (RFP)
A sample of a bed management RFP covering all the basics. Download the document and tailor it to your needs.
Advisory
An overview of Fiscal Year (FY) 2015 Hospital Value-Based Purchasing (VBP) Program.
Magazine & Journal Articles
Managing contract pricing more effectively—from creation to renewal or expiration—can deliver real operational and financial benefits for hea
Letter/Comment
On November 21, 2013, AHRMM submitted electronically
Advisory
An overview of the Centers for Medicare & Medicaid Services' three final rules for calendar year 2011 the outpatient prospective payment