how do you perform reverse enginearing study for drug containing sodium chloride sodium citrate sodium bicarbonate
1 4428Is it necessary to validate both assay and related substances for usp official methods for products.
6 13930Post New Analytical Chemistry Questions
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
how the compound separate in coulunm,explain
How to set specification of assay, fisdolution and related substances?
Difference between hlaf and rlaf
what is mean by peak intigrity?
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
Please give idea about method development for cleaning method and how maco level establish
As per ICH related substances stability trend limit from initial to shelf life
Why acetonitrile and water are used as extraction solvent when analysis melamine? I thought they are miscible and won't be able to separate...
sop of a uv visible spectrophotometer double beam elico model
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
what is definition of validation? which components are followed give detail?
function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?
In Dissolution Test why limit is define Q+5% what is the role of +5%.
why salisylic acid not using now days for disdolution calibration?