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Answer Posted / yojana
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How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
What is mean by PDR?
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
How would you decide dissolution medium for NCE compound of class I drug
if instrument calibration fails then what require to do?
which are the sizes of capsules?
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?
why we use glass fiber filters use in some situation?
what are the guidelines for analytical method validations?
why xterra column require to use at higher ph?
when we talk about change in entropy we consider total entropy means of surround +entropy of system but when we talk about change in Gibss free energy we consider entropy of system.explain with reason.
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
How we choose the mobile phase for method development.?
how you confirm the assay method?
