- US Pharmacopeia (USP)
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 Reference Standards
Recognized globally, USP Standards accelerate the pharmaceutical drug development process and increase confidence in the accuracy of analytical results USP Standards are built on deep science, provide a high degree of analytic rigor and are accepted by regulators around the world
- FAQs: USP and its Standards
USP’s primary compendia of standards are the United States Pharmacopeia and the National Formulary (USP–NF) USP standards may be adapted or adopted by any organization or government worldwide
- USP Convention
With over 450 Member Organizations from around the world, representing the full continuum of the pharmaceutical supply chain, the USP Convention provides a breadth and depth of critical perspectives that help shape and inform USP’s strategic focus
- Frequently Asked Questions (FAQs) | USP
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
- USP Verification Services
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
- What is a USP Monograph
Learn the definition of a USP monograph, how monographs are developed and how they effect quality prescription drugs
- USP–India
Learn about USP-India and how they allow USP to pursue collaborative opportunities with policy makers, regulators, professional and manufacturing associations, and leaders in India's pharmaceutical and food sectors
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