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why we use prednisone tablet in chemical callibration of
dissolution apparatus?
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Answer Posted / ritesh pandey
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about method developement in hplc
why xterra column require to use at higher ph?
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
which situation gc hs and gc als require to use?
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
what is mean by covalidation
What is the diffrence in japan mkt requirement in analytical method validation over US?
in api coa contains only process impurities and in product coa contains degradation impurities?
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
process of Diclofenac sodium,IP.
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
why salisylic acid not using now days for disdolution calibration?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
Why sometime potassium ortho phosphate mix with acetone use for sample preparation for hplc
