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16 Results Found
AHA Response to OMB Deregulation RFI
AHA responds to the Office of Management and Budget Deregulation Request for Information.
AHA Comments on Commerce Department Investigation of Pharmaceutical Imports
AHA comments on the Department of Commerce’s request for public comment on its Section 232 national security investigation on pharmaceutical and pharmaceutical ingredient imports.
AHA Responds to Commerce Department Investigation of Critical Minerals
AHA comments on the Department of Commerce’s request for public comment on its Section 232 national security investigation on processed critical minerals and derivative products.
AHA Urges Administration to Grant Exceptions for Tariffs for Medications and Medical Supplies
The AHA asks President Trump to consider granting exceptions to the current and proposed tariffs for medical devices and pharmaceuticals made in Mexico, Canada and China that are essential to the provision of safe, effective care in America's hospitals, clinics, and other settings.
AHA Comments to MedPAC on Rural Medicare Beneficiary Cost-sharing
February 28, 2025Michael Chernew, Ph.D.ChairmanMedicare Payment Advisory Commission425 I Street, NW, Suite 701Washington, D.C. 20001Dear Dr. Chernew:
AHA Comments to CMS on Financial Assistance Program Navigators
AHA response to CMS's request for comment on how navigators and non-navigator assistance personnel working within hospitals and health systems may help consumers access financial assistance programs to help pay for health care services.
AHA to President Urging the Administration to Take Action to Address IV Solution Supply Shortage as a Result of Helene
AHA letter to President Biden urging the Administration to take action to address IV solution supply shortage as a result of hurricane Helene.
AHRMM LUC Comments to the FDA’s Draft Guidance for Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices
The AHRMM LUC members submitted comments and recommendations to the FDA's Draft Guidance for Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices.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.
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 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