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USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
2020is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
2180we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion
1874Post New Analytical Chemistry Questions
if content uniformity passing but dissolution varrying then what is next step?
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
In which situation we require to prepare the standard solution from sample in Related substance method?
Why use only methanol,used determinationof moisture content not use other solvents
why we use a particular hplc column for a particular compound give reasons?please
what is classification of elemental impurities? what is risk assement in elemental impurities?
how to calibrate hplc & gc
In rs method development when we are going area normalization method to dilute standard method?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
if rsd failed then what require to do?
if you have given a blank water how you analyse by general analytical techniques?
why we are using hexane in calibration of number of drop per mL
about method developement in hplc
Which products will produce when acetic anhydride reacts with Ter-butanol, Sec-butanol, Iso butanol, Dimethylamine etc.
What is delay volume?
