Answer Posted / mohit thummar
*Q is the amount of dissolved active ingredient specified in the individual
monograph, expressed as a percentage of the labeled content.
| Is This Answer Correct ? | 5 Yes | 0 No |
Post New Answer View All Answers
why we are using hexane in calibration of number of drop per mL
4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
in which situation require to change rs specification?
Loss of linearity in tkn analysis, possible reasons?
why we use a particular hplc column for a particular compound give reasons?please
How to do regeneration of Metacarb Pb plus column?
[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
if content uniformity passing but dissolution varrying then what is next step?
Why are use silicon oil mr?
before starting analytical method valodation what you checking? and how giving preference to start validation?
What is similarity factor and its use in api strength?
what is mean by 40 in the dissolution basket mesh size?
pharma industries oriented