USP and Public Policy

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USP appreciates the opportunity to comment on the National Institute for Occupational Safety and Health (NIOSH) of the Centers for Disease Control and Prevention (CDC) draft document, Managing… Learn More
USP appreciates the opportunity to provide comments to the Food and Drug Administration (FDA or Agency) on the “Importation of Prescription Drugs” proposed rule. Learn More
USP appreciates this opportunity to present our comments on the competitive marketplace for biosimilars. Learn More
USP appreciates the opportunity to provide comments on FDA’s draft guidance, “Compounding Animal Drugs from Bulk Drug Substances.” Learn More
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USP appreciates the opportunity to comment on FDA’s draft guidance, “Clinical Immunogenicity Considerations for Biosimilar and Interchangeable Insulin Products.” Learn More
USP appreciates the opportunity to comment on the U.S. Hemp Authority Certification Program Standard v3.0 DRAFT. Learn More
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 appreciates the opportunity to on Health Canada's Controlled Substances and Cannabis Branch regarding quality issues of cannabis. Learn More
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