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using gradient pressure in gas chromatography are not ?using gradient pressure why
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
acceptance criteria for lod & loq by standard deviation of response and slope??
identification is for unknown? qualification for known? reporting for LOQ?
As per ICH related substances stability trend limit from initial to shelf life
Which parameters require to do in tech transfer?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
on the basis of bcs class how to proceed the solubility?
In the HPLC Calibration done wavelength accuracy done between 200nm-280nm .but not done remaining 300-400nm not done ?
if rsd failed then what require to do?
if you get peak in blank then what require to do?
How to determine the EDTA content by potentiometry titration in Ceftriaxine sodium
UV and PDA detector, which have less signal to noise ratio?
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
