Franciscan Missionaries of Our Lady Health System (FMOLHS)-GS1 US Data Standards Master Process Implementation Plan

By AHRMM

Related Resources

Letter/Comment
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 Fo
Advisory
CMS Releases Proposed Rule for Hospital Value-Based Purchasing Program
The Patient Protection and Affordable Care Act of 2010 (ACA) requires the Secretary of Health and Human Services to establish a VBP program t
Guides/Reports
Supply Chain Services Professional's Role in Achieving the Institute of Medicine's Six Aims for Improvement
In 2001 the Institute of Medicine (IOM) published
Letter/Comment
AHRMM Comment Letter to FDA Regarding the Draft Guidance for Industry on the Global Unique Device Identification Database (GUDID)
On November 21, 2013, AHRMM submitted electronically
Toolkits/Methodology
Guidance for Writing Comments
How to write a constructive, information-rich comment that clearly communicates and supports its claims to have an impact on regulatory decision…
AHRMM Leading Practice Statement on Supply Chain Integration
As a Leading Practice, the AHRMM Board of Directors adopts that Supply Chain Services be fully integrated into high cost clinical services…