Andrea Charles | 12/24/2010
Qualification of equipment and validation of analytical methods are critical components for the implementation of process analytical technology (PAT). Martin Warman, Scientific Fellow, Analytical Development at Vertex Pharmaceuticals, joins Andrea Charles from Pharma IQ, to discuss the effects of apply PAT to pharmaceutical manufacturing and how to successfully validate PAT methods. Warman also shares his insights on how to select the right partner in the validation process...
To continue reading this story Click Here
RECOMMENDED
MSD announces Phase III data on investigational treatment to lower LDL Cholesterol (LDL-C)
2025-11-17
AI for Pharma & Healthcare 2025
2025-06-18
Upcoming Events
Pharma Contract Manufacturing
23 - 25 March 2026
Mercure Hotel MOA Berlin, Germany
Register Now |
View Agenda |
Learn More