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wen v have polr solvent then which type of column use in hplc
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why multimedia dissolution require to do?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
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?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
what is biorelivent dissolution media?
what is mean by covalidation
function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?
what is mean by dissolution hydrodynamics?
What is related substance by HPLC impurity limits as per USP?
what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
for which product require to do content uniformity? what is limit of cu?
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?
