Answer Posted / ram krishna
Primary standard are highly purify and none degradable
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
How to start the dissolution development for unknown tab?
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
What should be the level/ Percentage of Arsenic in Arsenic free zinc.
Colorimtry
if identification threshold crosses the limits then what next step?
WHY given much noise PDA dector then VWD Dector
How would you decide dissolution medium for NCE compound of class I drug
which batch require to use for analytical method validation?
How to set analyticl specification for combination products?
if you get peak in blank then what require to do?
How you develop a method in HPLC?
what are the guidelines for analytical method validations?
in hplc chromatogram started from left to right and in uv spectrum started from left to right
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
if content uniformity passing but dissolution varrying then what is next step?
