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Qc interview questions
in which situation require to take incident in validation?
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?
function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?
why are measure gas flow " ml " in Gas chromatography
in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
why we use a particular hplc column for a particular compound give reasons?please
From where require to take the RLD sample?
using gradient pressure in gas chromatography are not ?using gradient pressure why
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
WHAT IS THE CRITERIA FOR SELECTION OF TIME OF DISSOLUTION AND THE MEDIUM OF DISSOLUTION?
why require to add enzymes in capsules dissolution only? is it require to tablet also?
How we choose the mobile phase for method development.?
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
