How to decide impurities in API & Drug Products and their release and shelf life specification
26:07
How to define limit for unknown, known and total impurities
17:16
How to Define Limit For Newly Identified Nitrosamine Impurity?
57:15
Evaluation of Elemental Impurities in Drugs and Drug Products ICH Q3D(R2)
17:09
What is Photostability and how to conduct it?
8:41
ICH Q3A l Impurities in New Drug substance l impurities in pharma industry l Question and answers
39:13
Impurities in Drug Substances/Products: Global Guidances & USP Perspective
20:38
Residual Solvents and Elemental Impurities: Classification & Exposure Limits as per ICH Q3C AND Q3D
20:04