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Post-Acute Care Advocacy Alliance News Update March 9, 2023
Post-Acute Care Advocacy Alliance Update for March 9, 2023.
CMS Releases FY 2024 Long-term Care Hospital PPS Proposed Rule
The Centers for Medicare & Medicaid Services (CMS) on April 10 issued the proposed rule for the inpatient and long-term care hospital (LTCH) prospective payment systems (PPS) for fiscal year (FY) 2024.
AHA Comments on March 2023 MedPAC Meeting Topics – Wage Index, Ambulatory Payments and Part D Drugs
AHA comments on three topics that were discussed during the March 2023 Medicare Payment Advisory Commission public meeting: the hospital wage index, alignment of payment rates across ambulatory settings and Medicare Part B drug payments.
AHA Comment Letter to DEA on Buprenorphine Telemedicine Prescribing Proposed Rule
AHA provides feedback on the Drug Enforcement Administration’s (DEA’s) proposed rule for expansion of induction of buprenorphine via telemedicine encounter.
AHA Support of FDA Blood Donation Eligibility Proposed Regulation
AHA comments on the FDA's draft guidance proposing that blood donor eligibility be determined based on individual risk assessment, regardless of gender or sexual orientation.
Maternal and Child Health Provisions Enacted in FY 2023 Omnibus Appropriations Package
The Consolidated Appropriations Act of 2023 (PL 117-328), signed into law in December 2022, contained a number of important maternal and child health provisions supported by the AHA.
AHA Comments on Proposed Revisions to the Regulations Governing the Confidentiality Of Substance Use Disorder Records
AHA comments proposed revisions to the regulations governing the confidentiality of substance use disorder (SUD) records, commonly known as 42 CFR Part 2 (“Part 2”).
AHA Comments on the CMS’ Request for Information on Essential Health Benefits (EHB)
AHA comments on the CMS’ Request for Information on Essential Health Benefits (EHB).
Better Health for Mothers and Babies
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FDA Issues Draft Guidance Updating Blood Donation Policy
The Food and Drug Administration (FDA) Jan.