Answer Posted / swati
We can qualify unknown impurity in RS method by spiking standard component in placebo...preparing sample solutions for accuracy and linearity depending upon specification limit of unknown impurity.
| Is This Answer Correct ? | 0 Yes | 2 No |
Post New Answer View All Answers
what is mean by peak intigrity?
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
Why six unit used for precision?
how to calculate elemental impurities?
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
Why dissolution test is not performed in all of the products
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 % )
How to compare XRD graphs against standard and carry polymorpism study of API's by powder XRD method?
Which parameters require to do in tech transfer?
for inorganic molecules require to do RS, Assay and disso?
why are measure gas flow " ml " in Gas chromatography
Difference between the quantitative analysis and qualitative analysis?
if you get peak in blank then what require to do?