// 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
// May 03, 2018
Solutions to help ensure biopharmaceutical quality
By the year 2020, biopharmaceuticals are estimated to account for 50% of the most successful phar
// March 01, 2018
Standards are evolving to help industry produce complex, quality assured biologic medicines
Highly complex biologics such as proteins, monoclonal antibodies, and cell and gene therapies inc
// November 24, 2015
USP Q&A: Dissolution, Disintegration and Drug Release Tests
USP Principal Scientific Liaison Margareth Marques, Ph.D., provides answers to questi
