USP and Public Policy
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USP Comment Letter: Submitted to Office of the United States Trade Representative on Comments on Promoting Supply Chain Resilience (USTR-20240002) (2024)
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The USP submits comments to the Draft Guidance for Industry; Dietary Supplements: New Dietary Ingredient Notifications and Related Issues (“Guidance”) published by the Food and Drug Administration (…
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USP Comment Letter submitted to Centers for Medicare & Medicaid Services (CMS) in response to the proposed rule “Patient Protection and Affordable Care Act, HHS Notice of Benefit and Payment…
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USP appreciates the opportunity to comment on the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) Q13 harmonized guideline draft.
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USP Comment Letter: Submitted to Canadian Food Inspection Agency on Proposed SFCA Regulations (2017)
USP appreciates this opportunity to submit comments on the proposed Safe Food for Canadians Regulations (the Proposed Regulations).
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Submitted on September 18, 2017 - USP Comment Letter to FDA in conjunction with the July 18, 2017 meeting on “Administering the Hatch-Waxman Amendments: Ensuring a Balance Between Innovation and…
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USP letter provided support to the efforts of WHO’s INN expert group to develop a consensus-based global approach to the naming of all biologicals that is consistent with existing, accepted…
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USP Statement to the WHO on the quality of hand sanitizers, or handrubs, as related to public health emergencies: preparedness and response.
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USP comments to FDA on “FDA Food Safety Modernization Act: Focus on Inspections and Compliance” Docket No. FDA-2011-N-0366. Comments were submitted in 2011.
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USP comments to FDA on “Periodic Review of Existing Regulations: Retrospective Review Under E.O. 13563.” Docket No. FDA–2011–N–0259. Comments were submitted in 2019.
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