// 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
// November 24, 2015
USP Q&A: Dissolution, Disintegration and Drug Release Tests
USP Principal Scientific Liaison Margareth Marques, Ph.D., provides answers to questi
// August 13, 2015
USP Strengthens Relationship with China to Improve Quality of Medicines and Food
Many of the drug ingredients used in generic medicines around the world are produced in China, an
