What is the difference between low pressure gredient and high pressure gredient in hplc instrument?
4 15136Generally for Normal Phase HPLC,stationary phase is Polar.In place of polar if we take non-polar means what happened & why?
7 15908Post New Analytical Chemistry Questions
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)
How to calibration of the uv spectroscopy and its test?
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
Which parameters require to do in tech transfer?
which situation gc hs and gc als require to use?
what is mean by ambient temperature?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
In which situation we require to analytical method validation of excipient?
Related substance method equivalency on control sample or spiked sample?
[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?