// 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
// 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
// November 24, 2015
USP Q&A: Dissolution, Disintegration and Drug Release Tests
USP Principal Scientific Liaison Margareth Marques, Ph.D., provides answers to questi
// October 26, 2015
The Evolving Role of Glycosylation Analysis for Biopharmaceuticals
By: Trish Li and Edith Chang
