about method developement in hplc
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What is impurities in pharma analysis?
In chromatograpbic purity 90% is there, in assay 70% is there. How will you prove remaining 30%.
how to calculate corelation coefficient in G.C Calibration? what is the calculation part?
In method developement or in any analysis if we use small length column for analysis what happen then ? why ?
how a particular wavelength can be different for a particular compund while analysing by uv and by HPLC.
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
why we use kbr as constant in the FTIR ?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
1 Answers Cipla, Elder, Vamsi Labs,
What is the difference between void volume and delay volume in HPLC?
Wt s the use of linearity in HPLC method validation
what are risk assement in the analytical qbd?
why do we use around only 60 mg of K2cr2o7 in the UV calibration -control of absorbance test?