analytical method validation require to with respect to release specification or shelf life specification?
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we 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
what is the criteria for choosing capillary column in GC??is it dependent on sample load?
function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?
why in GC calibration of linearity regression coefficient should not be less than 0.999
Why do we use KCl ,K2Cr207,Toulene & Halonium oxide for the caliberation of UV
What should be the precision for HPLC during technology transfer?
in dissolution why pool sample needed? in which type of drug pool sample need?
In Analytical method development related substance method when did follow w/w method when did follow area normalisation method
how to get accurate result for Residue on evaporation in purified water
why chiral compounds will rotate the plane polarized light in SoR.
What is difference between" LOD" AND "VACCUME LOD"
How to calibration of the uv spectroscopy and its test?