USP currently offers more than 3,500 Reference Standards—highly characterized specimens of drug substances, excipients, food ingredients, impurities, degradation products, dietary …

Explore USP's reference standards for ensuring quality and accuracy in pharmaceuticals, dietary supplements, and food products.

The USP Reference standards section of an individual USP or NF monograph or general chapter names each USP Reference Standard required for assay and test procedures and refers to …

Aug 19, 2020 · USP: US Pharmacopeia (USP) international organization defines reference standard materials as highly characterized specimens of drug substances, excipients, …

Apr 28, 2021 · Newly Available USP Reference Standards (updated as of April 28, 2021) The following USP RS, which were not available when the associated monograph was made …

Reference Standards provided by the United States Pharmacopeial Convention (USP Reference Standards or USP RS) are highly characterized physical materials or digital data demonstrated …

The QSS is a single resource that integrates monographs associated with an API or Excipient with all relevant general chapters, Reference Standards, Pharmaceutical Analytical Impurities …

All information required for the official use of a USP Reference Standard is provided in the associated USP compendial procedure, the label of the RS, and on its USP Certificate, if …

Mar 25, 2016 · USP currently offers more than 3,500 Reference Standards, including materials for drug substances, biologics, excipients, dietary supplements, food ingredients, impurities, …

USP Reference Standards are authentic specimens that have been approved by the USP Reference Standards Expert Committee as suitable for use as comparison standards in USP …