Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
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analytical method validation require to with respect to release specification or shelf life specification?
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
In burette calibration of Karl fischer Instrument, the multiplication factor 1.00693 is using for how much ml of water dispenced. why
As per ICH related substances stability trend limit from initial to shelf life
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why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
Why we are injecting low load standard conc. while analysing Related Substances by HPLC?
What is the use of tlc and hplc? And when and where use?
How long we can use hygroscopic reference standard in terms of water absorb.I mean in line with respective monograph's specification or more than that?
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?
In UV we measure absorbance , how it is happend ? explain me