Impurities in Drug Substances/Products: Global Guidances & USP Perspective
1:00:02
Nitrosamine Impurities | USP
1:01:49
Introduction to Analytical Quality by Design (AQbD) principles
1:02:17
Qualification of Dissolution Testers USP Performance Verification Test (PVT)
1:01:10
Determination of Metal Impurities in Pharmaceutical Products
58:50
Validation, Verification, & Transfer of Analytical Methods – USP General Chapters 1224, 1225 & 1226
1:31:06
The FDA Drug Development Process: GLP, GMP and GCP Regulations
15:03
How to decide impurities in API & Drug Products and their release and shelf life specification
1:05:03