One Raw material failed assay test is there any chance for failing purity of that material ?7 11781
What are the differences between GC and HPLC?1 14330
Why do we need GC instead of HPLC? or Why do we need HPLC instead of GC?4 11566
What is linearity in HPLC and how will you test?1 18819
What is the difference of time between two consecutive injections in HPLC?2 9721
Why we are use 0.005M Sulphuric acid, in control of absorbance performance test UV Spectrophotometer calibration2 14998
How much sample concentration should i inject against diluted standard in related substances for drug product in hplc analysis1 3660
how to prepare 25 ppm acetone. explian with formula4 16116
What is the diffeence between assay and uniformity of content2 8956
what is mean by peak intigrity?
what is biorelivent dissolution media?
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
How to start the dissolution development for unknown tab?
Is it nessesary all multimedia dissolution require descriminatory?
Why Ethanol is Used for Standardization of GC Head space?
Which is the highly polar and highly non polar column in HPLC?
why we should take dst factor for below 1%moisture samples
What is the difference between purge septum flow and column flow in gas chromatography?
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
Why six unit used for precision?
How do we fix the sample concentaryion in hplc method development?
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
in which situation require to take incident in validation?
In which situation we require to analytical method validation of excipient?