Why 10%,20%,30% Sucrose solution is used for the calibration
of polarimeter?
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How we choose the mobile phase for method development.?
could negative ions be produced by bombardment process in mass spectrometry?
what is mean by 40 in the dissolution basket mesh size?
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 ?
in which situation ion pair require to use?
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
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.
what is partion and column chromatography
how to decide for one product require water content or LOD?
how the compound separate in coulunm,explain
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
why require to do water content for drug product?
in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
Tell me about analytical method validation in QC
