Answer Posted / amol
zorbax,kromasil,thermo,waters, water symmetry,& many more
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analytical method validation require to with respect to release specification or shelf life specification?
What is similarity factor and its use in api strength?
how you fix the limits of impurities?
which are the sizes of capsules?
what is third integration
what is diffrence between specificity and selecivity?
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
mahagenco syllabus for the post of chemist
in dissolution why pool sample needed? in which type of drug pool sample need?
Please tell me about the pH of Polycaboxylic ether is it in the 5-6 range ever or more than 6
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
Ph meter can show more than 14 ph reading? Why ph range in between 1 to 14 only?
why require to add enzymes in capsules dissolution only? is it require to tablet also?
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.
if identification threshold crosses the limits then what next step?
