Reference Standards

New USP Standards for Characterization of Therapeutic Proteins

New USP Standards for Proteins

Learn about and view the new suite of physical and written standards that USP is developing to help biologics manufacturers develop and analyze therapeutic proteins. New general chapters address analytical procedures for monoclonal antibodies, oligosaccharides, and protein determination.

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Top 5 of 2015: Most-Read Quality Matters Blog Posts

Top Five Quality Matters Blog Posts of 2015

Thank you for helping Quality Matters spread the word in 2015 about USP quality standards and the important role our work plays in industry, public health and lives around the world. These five posts are the ones that you, our readers, found to be the most engaging and useful in 2015. 

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USP Q&A: Dissolution, Disintegration and Drug Release Tests

Answers to Common Questions about USP Standards for Dissolution, Disintegration and Drug Release Tests

Dissolution, disintegration and drug release tests are important tools during the entire lifecycle of a drug product, from early development throughout its shelf life. USP’s Margareth Marques, Ph.D., provides answers to common questions and insight into standards and resources for these tests. 

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