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Answer Posted / rakhi
no unit
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if you given one product then which tests you will perform?
As per ICH related substances stability trend limit from initial to shelf life
what is the disso medium for tropsiun chloride
How doing qbd practically?
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
In the HPLC Calibration done wavelength accuracy done between 200nm-280nm .but not done remaining 300-400nm not done ?
In BP2013, Loperamid HCl monograph. Assay by titration with 0.1N sodium hydroxide using hydrocloric acid 0.01N and reading the volume added between the 2 points of inflexion. I have a question that if the diluent solvent is ethanol is certainly consumed a amount of volume of titrant, so this volume must be eliminated on the result calculation or not apart from first point which is subtracted above.
mode of absorption in alimentary canal?
which batch require to use for analytical method validation?
How to calibration of the uv spectroscopy and its test?
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what are risk assement in the analytical qbd?
if you have given a blank water how you analyse by general analytical techniques?
what is the purge flow & how to calculate
