USP and Public Policy

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USP Comment Letter: Submission to ITC on Investigation No. 332-580; COVID-19 Related Goods: The U.S. Industry, Market, Trade, and Supply Chain Challenges (2020)
USP supports more transparency from the pharmaceutical industry to support a more resilient supply chain to help ensure the continued availability of safe, quality medicines. Learn More
USP Comment Letter: Submitted to FDA on Clinical Immunogenicity Insulin Draft Guidance (2020)
USP appreciates the opportunity to comment on FDA’s draft guidance, “Clinical Immunogenicity Considerations for Biosimilar and Interchangeable Insulin Products.” Learn More
USP Comment Letter: Submitted to US Hemp Authority Certification Program Standard (2020)
USP appreciates the opportunity to comment on the U.S. Hemp Authority Certification Program Standard v3.0 DRAFT. Learn More
USP Comment Letter: Submitted to HHS/ASPR/DSNS on Strategic National Stockpile (SNS) (2020)
USP appreciates the opportunity to provide comments in response to the request for information (RFI) from HHS/ASPR/DSNSS on the Strategic National Stockpile (SNS). Learn More
USP Comment Letter: Submitted to Health Canada on Cannabis Standards (2020)
USP appreciates the opportunity to on Health Canada's Controlled Substances and Cannabis Branch regarding quality issues of cannabis. Learn More
USP Comment Letter: Submitted to FDA on Fixed-Quantity Unit-of-Use Blister Packaging for Certain Immediate-Release Opioid Analgesics for Treatment of Acute Pain (2019)
USP appreciates the opportunity to respond to the U.S. Food and Drug Administration's (FDA's) Request for Comments on Fixed-Quantity Unit-of-Use Blister Packaging for Certain Immediate-… Learn More
USP Comment Letter: Submitted to FDA on Horizontal Approaches to Food Standards of Identity (SOI) Modernization (2019)
USP appreciates the opportunity to submit comments on the horizontal approaches to food standards of identity (SOI) modernization. These comments are being submitted on behalf of the Food Science… Learn More
USP Testimony: Submitted to FDA on Modernizing Standards of Identity (SOI) (2019)
USP appreciates this opportunity to discuss modernizing Standards of Identity (SOI) and the use of a horizontal approach to modernization. Learn More
USP Comment Letter: Submitted to FDA on Insulin Biosimilars (2019)
USP appreciates the opportunity to comment on “The Future of Insulin Biosimilars: Increasing Access and Facilitating the Efficient Development of Insulin Biosimilar and Interchangeable Products”. Learn More
USP Comment Letter: Submitted to FDA ‘Standards Development and the Use of Standards in Regulatory Submissions Reviewed in the Center for Biologics Evaluation and Research; Guidance for Industry (2019)
USP appreciates the opportunity to comment on the Food and Drug Administration’s (FDA or the Agency) final guidance, “Standards Development and the Use of Standards in Regulatory Submissions Reviewed… Learn More

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