Learn about USP’s portfolio of solutions to help address quality assurance, enhance regulatory predictability, and help manufacturers distribute quality medicines, dietary supplements and foods.

USP currently offers more than 3,500 Reference Standards—highly characterized specimens of drug substances, excipients, food ingredients, impurities, degradation products, dietary supplements, compendial reagents and performance calibrators.

Esta página web es un recurso destinado a los usuarios de USP de habla hispana. Contiene información actualizada útil con respecto a las normas y estándares USP, y otras novedades de diversa índole.

USP provides answers to Frequently Asked Questions (FAQs) as a service to stakeholders and others who are seeking information regarding USP’s organization, standards, standards-setting process, and other activities.

For over 200 years, USP has worked to build trust where it matters most: in the world's medicines, dietary supplements and foods. Through our rigorous science and the public quality standards we set, USP helps protect patient safety and improve the health of people around the world.

USP ofrece actualmente más de 3500 Estándares de Referencia: muestras con un gran nivel de caracterización de medicamentos, excipientes, ingredientes alimenticios, impurezas, productos de degradación, suplementos dietéticos, reactivos farmacopeicos y calibradores de desempeño.

Learn about USP’s portfolio of solutions to help address quality assurance, enhance regulatory predictability, and help manufacturers distribute quality medicines, dietary supplements and foods. Search and buy reference standards

2015年7月14日 · A USP Reference Standard (also known as a physical standard) is a known quantity of a drug substance or ingredient, developed in alignment with the specifications outlined in the USP–NF. These standards come in small vials, and enable pharmaceutical manufacturers to test their product against USP’s standards to ensure it meets published ...

USP Reference Standards of the General Notices and Requirements in the USP-NF online publication: “Where USP or NF tests or assays call for the use of a USP Reference Standard, only those results obtained using the specified USP Reference Standard are conclusive.”

2015年12月17日 · In 1938, the Food, Drug and Cosmetic Act reaffirmed the role of the pharmacopeia and expanded its role to include USP standards for labeling and packaging. Today, drugs sold in the United States are required to meet USP standards regardless of whether they include the letters “USP” on the label.