how we do assay of urea, ammonium sulpate, ammonium nitro
pospate etc
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why multimedia dissolution require to do?
Basic principle of ESI?
How we can identify process related and degradation impurity in single method with short period?
in dissolution why pool sample needed? in which type of drug pool sample need?
in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
How to start the dissolution development for unknown tab?
Which parameters require to do in tech transfer?
What is the difference between purge septum flow and column flow in gas chromatography?
why does used dry caffien in HPLC calibration?
What is column in chromatography?
what are risk assement in the analytical qbd?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
What is the principle of HPLC, GC, LCMS, GCMS,LC QQQ, GC QQQ, LC Q TOF and GC Q TOF. What are the applications and Specificity?