in dissolution in one tablets two molecule one is losartan &
second is HCTZ
losartam is complies in s1 stage & hctz is complies in s2
stage
then how to report result
losartan s1 stage result or losartan s2 stage result
Chromatographic Purity is a Qualitative analysis
why cone formation during dissolution?
we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion
How to establish relative response factor for hplc. Why it is required?
what is the difference between system precision and method precision?
3 Answers Teva Pharmaceuticals,
what is the difference between BDS and ODS Columens and both are same or not
2 Answers Intas, IPQA, Micro Labs, Vasava Engineering Private Limited,
What is the use of ELSD in HPLC?
What is Rf value& Rx value in TLC?
why are not used methonol in kf titrator to find out water content in ketones?
if you have given one product then how you determine the impurity in that?
Is it necessary to inject three replicate for accuracy in AMV.
What is FDA form 482c?