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?
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If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
In rs method development when we are going area normalization method to dilute standard method?
if you have given one product then how you determine the impurity in that?
why glutent are detected in the rice cereal baby food product even manufacturer claimed that they are using rice and milk only?we have using ELISA to do the test,and rice supposed not containing any glutent,rite?We already repeat the test so many times and it still detected.just wondering where the glutent came from?
how to select short coloum and long coloumn for new molecule
why multimedia dissolution require to do?
why digestion require in icpms?
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
could negative ions be produced by bombardment process in mass spectrometry?
how we can identify the impurity is coming below loq at transfering site?
If combination product how require to identify which imp is of which api?
why we are using hexane in calibration of number of drop per mL
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
Which is the highly polar and highly non polar column in HPLC?
why octanol used to determine the partition coefficient ?