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sodium vapour lamp
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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.
From where require to take the RLD sample?
what is the different in Total ash, sulphated ash, acid insoluble ash, alcoholic or non alcoholic ash?
if content uniformity passing but dissolution varrying then what is next step?
for inorganic molecules require to do RS, Assay and disso?
why we use Dichlorobenzene.nitrobezine.t-butyldi sulhate.for calibration of gc Head space
How we can identify process related and degradation impurity in single method with short period?
Difference between the quantitative analysis and qualitative analysis?
Which are the diffrent grades of api in pharma?
How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
Why use only methanol,used determinationof moisture content not use other solvents
In IR spectra, generally a molecule vibrates without apply emr or ir light?
why cone formation during dissolution?
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
