Why 10%,20%,30% Sucrose solution is used for the calibration
of polarimeter?
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which are the sizes of capsules?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
What is related substance by HPLC impurity limits as per USP?
what you do when compound having dwel wavelength?
why octanol used to determine the partition coefficient ?
Loss of linearity in tkn analysis, possible reasons?
if content uniformity passing but dissolution varrying then what is next step?
what is %labelled amount in content uniformity of dosage unit and its calculation?
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
if peak get problamatic then what require to do?
what is partion and column chromatography
In which situation we require to analytical method validation of excipient?
what is classification of elemental impurities? what is risk assement in elemental impurities?
which situation gc hs and gc als require to use?
why cone formation during dissolution?
