Pharmaceuticals

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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The Evolving Role of Glycosylation Analysis for Biopharmaceuticals

New USP standards for glycosylation analysis

Learn about the evolving and challenging role of glycosylation analysis in biopharmaceutical science and how USP documentary and reference standards can support advances in this field.

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NCPIE Talk About Your Medicines Month: Discussing Safe Use, Storage & Disposal

October is NCPIE Talk About Your Medicines Month

October is Talk About Your Medicines Month. Sponsored by NCPIE, a USP Convention member organization, this annual opportunity encourages patients and healthcare providers to engage in conversation about medications and their safe use, safe storage, and safe disposal.

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