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Answer Posted / suri
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if identification threshold crosses the limits then what next step?
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?
how will you do the prep for unstable componds?
which situation gc hs and gc als require to use?
In which situation we require to prepare the standard solution from sample in Related substance method?
How to compare XRD graphs against standard and carry polymorpism study of API's by powder XRD method?
Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .
how you determine moist.of NaOH sol or NaOH flacks
UV and PDA detector, which have less signal to noise ratio?
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
What is gelatinization?
what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means
why require the ph, buffer during hplc mobile phase?
