Us Congress 2023-2024 Regular Session

Us Congress House Bill HB3093

Introduced
5/5/23  
Refer
5/5/23  

Caption

Affordable Pricing for Taxpayer-Funded Prescription Drugs Act of 2023

Impact

If enacted, HB3093 would have significant implications on how federal research funding is allocated and utilized. Biomedical products, including drugs, vaccines, and medical devices developed with government support would be subjected to pricing regulations to enhance public access to affordable healthcare. By potentially aligning U.S. prices with those in other wealthy nations, the bill intends to decrease financial burdens on patients and promote fairness in the pharmaceutical market. This could also affect research incentives, as developers might need to balance profit motives with compliance to these pricing structures.

Summary

House Bill 3093, known as the Affordable Pricing for Taxpayer-Funded Prescription Drugs Act of 2023, seeks to establish reasonable pricing agreements for biomedical products developed through federally funded research. The bill mandates that any biomedical product or service deriving from such funding must not be sold to U.S. residents at a higher price than what consumers pay in other high-income countries. This aims to ensure that taxpayer dollars are not used to inflate medical costs, thereby increasing access to healthcare for all citizens.

Contention

Debate surrounding HB3093 is expected to revolve around the tension between ensuring public affordability of biomedical products and protecting pharmaceutical innovation. Supporters argue that the bill will incentivize equitable pricing in an industry notoriously marked by high costs, while critics may raise concerns over how it could impact future research funding and the development of new drugs and therapies. The bill includes provisions for waivers under certain circumstances, which could also spark discussions on transparency and the public's ability to influence these waivers favorably.

Transparency

The bill emphasizes transparency by requiring manufacturers to report costs related to clinical trials and additional financial disclosures, fostering an environment where stakeholders can hold companies accountable for pricing practices. This aim for transparency is designed to strengthen the public interest, ensuring that innovations funded by taxpayers do not exploit pricing loopholes.

Companion Bills

No companion bills found.

Previously Filed As

US SB150

Affordable Prescriptions for Patients Act of 2023

US HB885

TRACK Act of 2023 Taxpayer Research And Contributions Knowledge Act of 2023

US SB113

Prescription Pricing for the People Act of 2023

US SB315

TRACK Act of 2023 Taxpayer Research And Contributions Knowledge Act of 2023

US HB2675

Affordable Payment Agreements for Taxpayers Act

US HB4322

Equal Dignity for Married Taxpayers Act of 2023

US HB4301

Bonding Reform and Taxpayer Protection Act of 2023

US HB3329

End Taxpayer Funding of Gender Experimentation Act of 2023

US HB8848

Affordable and Safe Prescription Drug Importation Act of 2024

US SB2221

Equal Dignity for Married Taxpayers Act of 2023

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