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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
how require to set assay concentration for standard and sample?
Who discovered X-ray
As per USP u/vacuum means (how much vacuum should be applied)?
what is the difference between qualitative analysis and quantitative analysis and explain them?
why do we adjusted ph in the mobilphase
Why potassium dichromate was using in Uv calibration?
What is dose dumping? why require to do?
perchloric acid&glacal acetic acid both are acids but reaction is complete in volumetric titrations.how?
what is Hilic chromatography?
Why do we use 500ppb sucrose and 500ppb 1,4 benzoquinone in TOC calibration?
Why 1800 ml of dissolution media used In Carbamazepine ER USP Tablets But other drug only 900 ml Media Used ?