CATEGORIES
Explore our wide range of reference materials organized into clear
categories making it easier for you
to find reliable solutions for testing, compliance, and research
needs.
USP’s APIs, Analytical Reference Materials (ARMs) with Reference Standard (RS) and PAIs, offers a complete solution to support diverse analytical applications across multiple therapeutic areas.
USP’s food analytical materials support accurate testing and quality assurance across diverse food and nutrition applications.
Discover PAIs and Analytical Reference Materials (ARMs) that help detect, manage, and control impurities, ensuring product safety from raw materials to release.
Comprehensive peptide and Monoclonal Antibody (mAb) solutions enable efficient method validation, equipment qualification, and faster biologics development.
USP’s standards and Analytical Reference Materials (ARMs) streamline regulatory compliance and tackle challenges in complex generics and formulations.
Access expanding excipient solutions Reference Standard (RS) and Analytical Reference Materials (ARMs) to meet regulatory expectations and overcome formulation hurdles.
USP's E&L System Suitability mixtures for GC-MS and LC-MS–electrospray ionization (ESI) facilitate manufacturers' ability to meet Good Manufacturing Practice requirements with confidence that the E&L screening data are robust, reproducible, and prepared for regulatory inspection. These system suitability mixtures bring consistency between setups and laboratories, confidence in analytical results, and ultimately help meet stringent regulatory expectations.
Backed by USP's scientific expertise in analytical research, biologics and synthetic chemistry, our materials drive quality throughout the drug lifecycle.
Each material is tested and released using rigorous processes developed by the same USP experts on staff who are involved with our trusted standard setting process.
Designed to help meet global regulatory requirements and support streamlined product approvals.
Brought to you by one of most trusted organizations, recognized by regulators and industries worldwide for our commitment to quality.
Ideal for method validation, system suitability, and impurity profiling in pharmaceutical testing.
