Pharmaceuticals

USP–NF Excipients: Challenges & Opportunities

Challenges and Opportunities in Updating USP-NF Excipients

Learn about USP’s comprehensive approaches for updating three high-priority excipient monographs—Guar Gum, Shellac, and Butylated Hydroxytoluene—the challenges encountered, and progress made implementing an initiative to develop up-to-date USP–NF excipient monographs.

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Pharmacopeial Forum: 5 Things You Should Know

What is PF and how to use it to change USP standards

Pharmacopeial Forum (PF) is the vehicle through which USP publishes proposed revisions to USP–NF standards for public review and comment. Learn about PF and how you can use it to help shape standards for drugs, excipients and dietary supplements.

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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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