One Raw material failed assay test is there any chance for failing purity of that material ?
7 11835Why we are use 0.005M Sulphuric acid, in control of absorbance performance test UV Spectrophotometer calibration
2 15036How much sample concentration should i inject against diluted standard in related substances for drug product in hplc analysis
1 3691Post New Analytical Chemistry Questions
What is mean by PDR?
what is mean by peak intigrity?
In which situation we require to prepare the standard solution from sample in Related substance method?
why we use glass fiber filters use in some situation?
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
What is diffrence between extractable volume and deliverable volume? Answer pls
Which parameter require to do for analytical method equivalency?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
what is the different in Total ash, sulphated ash, acid insoluble ash, alcoholic or non alcoholic ash?
how require to select dissolution media? what is discrimination?
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
process of Diclofenac sodium,IP.
What is similarity factor?
if you have given a blank water how you analyse by general analytical techniques?