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sodium vapour lamp
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analytical method validation require to with respect to release specification or shelf life specification?
why we use Dichlorobenzene.nitrobezine.t-butyldi sulhate.for calibration of gc Head space
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
What is related substance by HPLC impurity limits as per USP?
we can use expired sample for validation and analyst qualification?
for which product require to do content uniformity? what is limit of cu?
some product having water content method with pyridine and ethylene glycol mixture instead of methanol? how they are selecting and methanol is not suitable solvent how ?
what is the difference between potentiometric titration and karl fischer titration?
What is a difference between potency and purity?
What is the calibration of uv process and preparation
Why we check moisture,ash & AIA in product
how to qualify the impurity?
What is the use of tlc and hplc? And when and where use?
what is biorelivent dissolution media?
