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AHA Associate Program Homepage

Issue Landing Page
The American Hospital Association (AHA) Associate Program opens the door to new opportunities and connections with our most active and engaged healthcare executives.

Recent Guidance on Meaningful Use of EHRs Makes Compliance More Difficult

Letter/Comment
Recent Guidance on Meaningful Use of EHRs Makes Compliance More Difficult.

AHRMM Awareness Brief: Draft Guidance for UDI Convenience Kits

Issue Brief
This Awareness Brief provides a quick reference to the Draft G

AHRMM Comment Letter to FDA Regarding the Draft Guidance for Industry on the Global Unique Device Identification Database (GUDID)

Letter/Comment
On November 21, 2013, AHRMM submitted electronically

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

Letter/Comment
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 A
Public

Financial Fact Sheets

Financial fact sheets from AHA's Policy Research.
Member

Hospital Associations and Hospitals File Lawsuit Challenging Federal Rule That Ties Providers’ Hands

The American Hospital Association (AHA), joined by the Texas Hospital Association, Texas Health Resources, and United Regional Health Care System, today sued the federal government to bar enforcement of an unlawful, harmful, and counterproductive rule that has upended hospitals’ and health systems’ ability to share health care information with the communities they serve, analyze their own websites to enhance accessibility, and improve public health.

New Guidance on Humidity Levels in the Operating Room

Advisory
New Guidance on Humidity Levels in the Operating Room

Hospital Compare: CMS Suspends Display of Hospital-Acquired Conditions Data

Advisory
Hospital Compare: CMS Suspends Display of Hospital-Acquired Conditions Data

Global Unique Device Identification Database (GUDID) Draft Guidance for Industry

Letter/Comment
This page provides information about submitting data to the database for device Labelers, entities responsible for providing the data to the GUDID.