Report of the Catalog Number Work Group

Letters/Comments

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

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…

Advisories

Guidance on Humidity Levels in the Operating Room

Advisories

Special Fraud Alert: Physician-Owned Entities

This Special Fraud Alert focuses on the specific attributes and practices of PODs that OIG believes produce substantial fraud and abuse risk and pose…

Advisories

Statement on Pricing Transparency

AHRMM’s Issues & Legislative Committee issued the following Statement on Pricing Transparency approved by AHRMM Board of Directors:<

Advisories

FDA Releases Proposed Rule on Unique Device System for Medical Devices

The FDA UDI ruling has finally arrived - the proposed rule has published.