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how you establish the LOQ?
how to calibrate hplc & gc
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
In Assy by potentio metry titration method how select MET U ,DET U, SET U,
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
why holium oxide prepared in 10% HCLO4 SOLUTION
what is mean by ambient temperature?
How can I develope method of dissolution by HPLC OR UV
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?
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
In HPLC calibration, caffeine is used as primary standard for wave length calibration due to caffeine is having dual maxima at 273 & 205 nm and one minima at 245 nm. Any body can give reference of these details from any pharmacopeia (with chapter no.) or any other authentic guideline?
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
why require to do water content for drug product?
what is the different in Total ash, sulphated ash, acid insoluble ash, alcoholic or non alcoholic ash?
What is the acceptance criteria for moisture balance when calibrated with sodium sulfate
