Why we are use 0.005M Sulphuric acid, in control of absorbance performance test UV Spectrophotometer calibration
2 11430How much sample concentration should i inject against diluted standard in related substances for drug product in hplc analysis
1 1946Post New Analytical Chemistry Questions
What are modes of quantification in related substances
what is the structure of DOWEX-50
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
what is %labelled amount in content uniformity of dosage unit and its calculation?
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
What is the difference between known and unknown impurities?
As per ICH related substances stability trend limit from initial to shelf life
about method developement in hplc
WHY given much noise PDA dector then VWD Dector
Can we interpret accuracy from linearity in method validation?
how a particular wavelength can be different for a particular compund while analysing by uv and by HPLC.
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
