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Un-Answered Questions { Chemistry }

How doing qbd practically?

980


which situation gc hs and gc als require to use?

794


on saturation solubility study data how we can find out the bcs class of drug?

904


identification is for unknown? qualification for known? reporting for LOQ?

726


Which parameter require to do for analytical method equivalency?

787


what is biorelivent dissolution media?

814


in which situation require to change rs specification?

755


If combination product how require to identify which imp is of which api?

842


in which situation ion pair require to use?

825


What is shaking level in GC?

796


What is split ratio in Gc? Splitless? how requirr to select?

895


why digestion require in icpms?

778


[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?

796


How we can identify process related and degradation impurity in single method with short period?

826


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.?

717