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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

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Horacio Pappa
researcher working with samples
Medicines
 // March 13, 2017

Exploring Continuous Manufacturing Technology and Applications in the Pharmaceutical Industry

 

Medicines
 // 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

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Fouad Atouf, Ph.D.
Chromosomes
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

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