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What is the diffrence in japan mkt requirement in analytical method validation over US?
how can I make the copper get white bye any salt or acit?
what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
Why we check moisture,ash & AIA in product
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?
Why six unit used for precision?
is it nessesary to do solution stability for 7 days?
Why sodium hydroxide used for maintain pH of phosphate buffer
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
Why are use silicon oil mr?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
Why perchloric acid used for potentiometric titration
