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How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
how to develop the icp ms method? Application of icp ms?
What is the diffrence in japan mkt requirement in analytical method validation over US?
From where require to take the RLD sample?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?
if you have given one product then how you determine the impurity in that?
Is it nessesary all multimedia dissolution require descriminatory?
which are the sizes of capsules?
if content uniformity passing but dissolution varrying then what is next step?
what is classification of elemental impurities? what is risk assement in elemental impurities?
what are risk assement in the analytical qbd?
why multimedia dissolution require to do?
in OSD forms require to use gas chromatography?
why require to do water content for drug product?
