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USP Biologics™. USP Biologics is prioritizing the ongoing development of state-of-the-art analytical tools, standards and solutions to support regulatory predictability, allowing manufacturers to operate with a high level of confidence and certainty throughout the drug development and approval process across a variety of modalities.
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.
Reference Standards Catalog. 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. Click below to download the full list. Download as PDF. Download as Excel.
The United States Pharmacopeia (USP) is a pharmacopeia (compendium of drug information) for the United States published annually by the over 200-year old United States Pharmacopeial Convention (usually also called the USP), a nonprofit organization that owns the trademark and also owns the copyright on the pharmacopeia itself.
Aug 4, 2015 · You may not know about the United States Pharmacopeia (USP), but chances are you’ve been positively impacted by our activities. Here are some facts about who we are, what we do, and what it means to you. FACT: USP is the only independent, not-for-profit, nongovernmental pharmacopeia in the world.
Aug 7, 2014 · Few people understand the meaning or function of a pharmacopeia, but it plays an important role in safeguarding public health. The idea of documenting...
Jul 14, 2015 · FACT: There are two types of standards. Documentary standards (also known as monographs)—covering everything from developing a drug to storing it—appear in our reference text, the United States Pharmacopeia-National Formulary ( USP–NF ).
