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Answer Posted / bhanu pratap singh
michail tswett
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In which situation we require to analytical method validation of excipient?
if identification threshold crosses the limits then what next step?
is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
what is the difference between potentiometric titration and karl fischer titration?
if you given one product then which tests you will perform?
what is the origin to prepare standard operating procedure
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
why we are using benzene, anyline in acetic anhdride assay titration method?
What is the purpose of octyl silane columns?
what is diffrence between specificity and selecivity?
From where require to take the RLD sample?
What is mean by PDR?
pharma industries oriented
before starting analytical method valodation what you checking? and how giving preference to start validation?
why we use Dichlorobenzene.nitrobezine.t-butyldi sulhate.for calibration of gc Head space
