USP is dedicated to helping improve global health through standards setting in compounding, biologics, pharmaceutical manufacturing and other fields.

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 …

Developing documentary standards and Reference Standards is the core of what we do at USP. These standards help to assess the quality, strength, identity, and purity of chemical medicines, biologics, …

Important Update: The subscription prices for the USP–NF and other online products will be changed on your next license renewal cycle, starting October 1st, 2025. Click here to learn more.

May 1, 2023 · USP provides answers to Frequently Asked Questions (FAQs) as a service to stakeholders and others who are seeking information regarding USP’s organization, standards, …

USP’s Verification Programs are universally recognized as the trusted standard for verifying the quality of dietary supplements, dietary ingredients, active pharmaceutical ingredients (APIs) and excipients.

USP’s unbiased, science-based approach to standards-setting is one of the key reasons USP is viewed as one of the most credible sources of public quality standards for medicines.

Pharmaceutical Analytical Impurities All Therapeutic Areas Therapeutic Areas (A) Therapeutic Areas (B-M) Therapeutic Areas (N-Z) Subscriptions & Publications USP-NF Dietary Supplements Compendia …

Nov 8, 2022 · USP develops standards for preparing compounded sterile medications to help ensure patient benefit and reduce risks such as contamination, infection or incorrect dosing.

Learn the definition of a USP monograph, how monographs are developed and how they effect quality prescription drugs.