USP and Public Policy
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USP Comments to FDA Public Meeting: “The Hatch-Waxman Amendments: Ensuring a Balance Between Innovation and Access” Regarding Generic Medicines. Comments were submitted 7-18-2017.
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Submitted August 18, 2023 to Senators Sanders and Cassidy and Representatives McMorris-Rodgers and Pallone regarding the Request for Information Regarding the Food and Drug Administration Regulation…
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USP appreciates the opportunity to provide comments for the National Conference on Weights and Measures’ (NCWM) consideration on proposed commercial measurement standards for cannabis and cannabis-…
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Promoting geographic diversification of the manufacturing base for U.S. drug products can help reduce supply chain vulnerabilities. Published December 2023.
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USP supports comprehensive policies and programs to address AMR, including building capabilities among global stakeholders to reduce the proliferation of poor-quality medicines and advocating and…
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USP Global Public Policy Position published 2024
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The United States Pharmacopeia (USP) is pleased to support the “Mapping America’s Pharmaceutical Supply Act” (H.R. 6992), or the MAPS Act.
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Recently, media reports have highlighted the results of drug quality testing from some contract laboratories that are analyzing the quality attributes of human drug products using testing methods…
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101 signatures, including USP, wrote to express the collective strong desire to see the Pandemic and All-Hazards Preparedness Act (PAHPA) reauthorized before the end of the calendar year in the same…
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USP Comment Letter to Senators Sanders and Cassidy and Representatives McMorris-Rodgers and Pallone ( ranking members of the Senate HELP Committee and House Energy and Commerce Committee) regarding…
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