what is the difference between polarimeter lamp and ir lamp
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what is the maximum flow rate in prep hplc
what is reverse phase chromarography&normal phase chromatography
What are the parameters for the method development of Gas Chromatography and GC-HS?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
reasons for negative peaks in chromatography
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
why in GC calibration of linearity regression coefficient should not be less than 0.999
why we use polystyrene film for ftir calibration?
What is the reason for using the 900ml of dissolution medium
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
why r u using hplc grade solvents
Explain in detail what are the procedure and calculations involved for accuracy (%Recovery)in method validation?