// 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
// July 28, 2016
Strengthening Global Medicines Quality: USP’s New Role in Harmonization
Over the past three decades, our medicines have become increasingly “globalized.” In the US alone
// November 24, 2015
USP Q&A: Dissolution, Disintegration and Drug Release Tests
USP Principal Scientific Liaison Margareth Marques, Ph.D., provides answers to questi
// May 24, 2016
Pharmaceutical Manufacturing in LMICs: Where Things Go Wrong
The Root Causes of Substandard Medicines in Lower and Middle Income Countries (LMICs)
