How to decide impurities in API & Drug Products and their release and shelf life specification
12:21
How to Remove Carryover in HPLC?
57:15
Evaluation of Elemental Impurities in Drugs and Drug Products ICH Q3D(R2)
17:09
What is Photostability and how to conduct it?
12:24
10 Step Control Strategy to Avoid Nitrosamine Impurities
8:35
How to Decide the Need of Testing Nitrosamine Impurities into Pharmaceuticals?
32:14
Challenges during HPLC method development and how to fix them
21:16
ICH Q1A in Detail- Stability testing on New Drug Substance & Product
40:54