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Medicines
 // December 04, 2014

Discussing a Lifecycle Approach to Validation and Verification of Analytical Procedures

Validation and verification of analytical procedures are quality assurance activities with broad

Profile picture for user hp@usp.org
Horacio Pappa
researcher working with samples
Medicines
 // June 08, 2023

Insights from India: Q&A with USP nitrosamines expert

The issue of addressing potential nitrosamine impurities in medicines has been the focus at event

Mrunal Jaywant
Mrunal Jaywant
Speakers at USP's Workshop on Nitrosamines Impurities
Medicines
 // November 24, 2015

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

USP Principal Scientific Liaison Margareth Marques, Ph.D., provides answers to questi

M
Margareth Marques
Answers to Common Questions about USP Standards for Dissolution, Disintegration and Drug Release Tests
Biologics
 // October 26, 2015

The Evolving Role of Glycosylation Analysis for Biopharmaceuticals

By: Trish Li and Edith Chang

U
USP Staff
New USP standards for glycosylation analysis

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