AHA on July 21 submitted comments on how Congress can ensure that the 340B program continues to benefit patients and communities, while acting to prevent any cuts to the program that would jeopardize patient access to care. Responding to a bipartisan request by senators for input, AHA strongly urged that the Health Resources and Services Administration finalize its Administrative Dispute Resolution rule for the 340B program and explicitly state that the ADR process is an available forum for affected 340B hospitals to seek redress from restrictions targeted to community and specialty pharmacies. AHA also recommended that Congress require HRSA to increase its annual audits of drug companies in the 340B program, which average six per year compared with over 200 per year for 340B covered entities, and give hospitals and other covered entities the ability to audit drug manufacturers.

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The AHA Oct. 27 submitted comments on the Supporting Underserved and Strengthening Transparency, Accountability, and Integrity Now and for the Future of 340B…
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The U.S. District Court for the District of Maine should deny motions by several drug companies and Pharmaceutical Research and Manufacturers of America to…
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The AHA today voiced support () for the 340B Rebate Model Delay Act (H.R. 10770)in a letter to the bill’s House sponsors. The bipartisan bill would pause the…
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The AHA, the Maine Hospital Association and four safety-net hospitals Oct. 9 filed a lawsuit in the U.S. District Court for the District of Maine challenging…
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The AHA, the New Hampshire Hospital Association and 340B Health have filed an amicus brief supporting Mary Hitchcock Memorial Hospital’s request for a…
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The Department of Health and Human Services’ Health Resources and Services Administration Oct. 1 announced approval of 10 drug companies to participate in the…