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AHA Comments on the Remanufacturing of Medical Devices, Draft Guidance for Industry and FDA Staff
AHA comments on the Remanufacturing of Medical Devices, Draft Guidance for Industry and Food and Drug Administration Staff.
AHA, Others Urge UnitedHealth Group to Provide Breach Notifications on Behalf of the Field
May 8, 2024Andrew P. WittyChief Executive OfficerUnitedHealth GroupP.O. Box 1459Minneapolis, MN 55440-1459Dear Mr. Witty:
AHA Letter of Support for the Affordable Connectivity Program Extension Act of 2024
The AHA voices support of the Affordable Connectivity Program Extension Act of 2024 (S. 3565).
AHA Response to Representative Bera on Artificial Intelligence in the Health Care Sector
The AHA responds to Representative Bera's request for information regarding the current state of artificial intelligence in the health care sector.
Letter to CMS Administrator Brooks-LaSure on the Higher Spending on Two Catheter Codes and the Impact on ACOs
The undersigned organizations write to request that accountable care organizations (ACOs) are held harmless from anomalous Medicare spending outside their control, such as the aberrant billing for catheters experienced in 2023.
AHA Letter to House E&C Subcommittee for May 1 Hearing on Change Healthcare Cyberattack
April 29, 2024
AHA Letter to Senate Finance Committee for May 1 Hearing on Change Healthcare Cyberattack
April 29, 2024
AHA Supports Legislation to Continue Hospital-at-home Model
The American Hospital Association comments on the discussion draft of the Hospital Inpatient Services Modernization Act to extend the acute care hospital-at-home program.
AHRMM LUC Comments to the FDA’s Draft Guidance for Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices
The AHRMM LUC members submitted comments and recommendations to the FDA's Draft Guidance for Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices. They recommend that information related to all Class I Medical Devices be included in the GUDID without exception.
AHA Comments on CMS Proposal on Accrediting Organization Oversight
AHA comments on CMS’ proposals to strengthen the agency’s oversight of accrediting organizations.