How doing qbd practically?
which situation gc hs and gc als require to use?
on saturation solubility study data how we can find out the bcs class of drug?
identification is for unknown? qualification for known? reporting for LOQ?
Which parameter require to do for analytical method equivalency?
what is biorelivent dissolution media?
in which situation require to change rs specification?
If combination product how require to identify which imp is of which api?
in which situation ion pair require to use?
What is shaking level in GC?
What is split ratio in Gc? Splitless? how requirr to select?
why digestion require in icpms?
[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?
How we can identify process related and degradation impurity in single method with short period?
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
