Loss of linearity in tkn analysis, possible reasons?
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When we calculate Impurity against impurity std.solution and when we calculate impurity against diluted standard with applying RRF?
In UV calibration we use Holmium perchlorate solution made in 1.4M perchloric acid The question is that 1.4 M perchloric acid we make is it in water or glacial acetic acid?
what is peak purity? how may types of methods to determine peak purity?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
what is the difference between the ordinary loss on drying technique and vacuum oven technique?
why we get only one peak in assay by hplc but in rs by hplc get more peaks
what is the difference b/w water content & moisture content
What is the difference between ROI & sulphates ash?
if instrument calibration fails then what require to do?
wen v have polr solvent then which type of column use in hplc
how to develop the shorter run time for pharmacopeial methods having 100 min run time?
why you are using benzoic acid for water content determination in TEA