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New Guidance on Humidity Levels in the Operating Room
Advisory
New Guidance on Humidity Levels in the Operating Room
HRSA Finalizes 340B Administrative Dispute Resolution Process
The Department of Health and Human Services (HHS) and the Health Resources and Services Administration (HRSA) April 19 published the 340B Administrative Dispute Resolution (ADR) final rule establishing a process that was required under the Affordable Care Act.
AHA Statement on "Evaluating Approaches to Diagnostic Test Regulation and the Impact of FDA’s Proposed Rule."
AHA statement before the House Committee on Energy and Commerce
Subcommittee on Health on the impact of the Food and Drug Administration’s (FDA) proposed regulation of diagnostic tests.
AHA Urges Congress to Provide Support to Help Minimize Further Fallout from Change Healthcare Attack
We are now on day 13 of the crisis caused by the recent cyberattack on Change Healthcare and its impacts on hospitals, health systems and patients around the country. We urgently need Congress's support to help minimize further fallout from this attack.
Medical Device Excise Tax - What You Should Know
Issue Brief
The Medical Device Excise Tax, a component of the Affordable Care Act, is approaching implementation at the beginning of 2013.
Medical Device Tax Next Steps
Advisory
The medical device excise tax is a feature of the Affordable Care Act. It is important to be knowledgeable about the tax and its effects.
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AHRMM Awareness Brief: Draft Guidance for UDI Convenience Kits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
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