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How do you increase the number of theoretical plates?
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what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
why we should take dst factor for below 1%moisture samples
in which situation ion pair require to use?
how require to interprit the method precision data of hptlc?
on saturation solubility study data how we can find out the bcs class of drug?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
which batch require to use for analytical method validation?
how you confirm the assay method?
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
sop of a uv visible spectrophotometer double beam elico model
why require the ph, buffer during hplc mobile phase?
in stress study if your api not soluble in hcl naoh h2o2 then what require to do?
why salisylic acid not using now days for disdolution calibration?
