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CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
Loss of linearity in tkn analysis, possible reasons?
Did anybody have method for acetyl cysteine effervescnce tablet
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
How will u perform degradation study in detectors other thann PDA in HPLC Methodology
What is the diffrence in japan mkt requirement in analytical method validation over US?
how to select short coloum and long coloumn for new molecule
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
how you start the solubility study?
is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
Please tell me about the pH of Polycaboxylic ether is it in the 5-6 range ever or more than 6
Difference between the quantitative analysis and qualitative analysis?
on saturation solubility study data how we can find out the bcs class of drug?
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
