How did you conclude that when stressing a compond, all
degradation products have eluted in chromatogram?
Answer Posted / hemant
Method should be stability indicating & should give mass
balance
| Is This Answer Correct ? | 3 Yes | 0 No |
Post New Answer View All Answers
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
WHAT IS THE PARAMETER FOR THE SELECTION OF MOBILE PHASE IN HPLC?
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
identification is for unknown? qualification for known? reporting for LOQ?
on the basis of bcs class how to proceed the solubility?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
give clarity of linearity and range in method validation
all types of questions asked at the cipla interview
which situation gc hs and gc als require to use?
in which situation require to take incident in validation?
what are risk assement in the analytical qbd?
what is mean by extactable and leachable study?
which are the sizes of capsules?
How to calculate coreletion coefficient