What is intact assay method development.....?
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what is classification of elemental impurities? what is risk assement in elemental impurities?
if relative response factor is 1.07, to select how much value
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
How will u perform degradation study in detectors other thann PDA in HPLC Methodology
In UV-VIS spectrophotometer:My diluent is methanol even though i corrected base line for methanol,In my sample scan i found methanol peak.what is the reason?
A new drug substance found fail to meet specification for an unknown Impurity during stability study(Specific change),how would further proceed?
If we have a kc is1*10^8 and the .kp 2*10^5 of reaction A------->B C------->D what is the volume of C?
water is more polar than acetonitrile.but in reverse phase chromatography peaks elute earlier when we increse Acetonitrile.what is the reason.
Why forced degradation studies are performed in hplc method validation?
in hplc chromatogram started from left to right and in uv spectrum started from left to right
why we want incorporate area of each solution of Intermediate precision and repeatability as well as Accuracy ? What is the use to incorporate area of each solution of Intermediate precision and repeatability as well as Accuracy ?
Did anybody have method for acetyl cysteine effervescnce tablet