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Chemistry AllOther (190) [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?
851How we can identify process related and degradation impurity in single method with short period?
870inhouse 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.?
779
which gas is used in preaparation of bit salt
What is a difference between potency and purity?
cefoperozone and sulbactam inj. hplc test method
What is split ratio in Gc? Splitless? how requirr to select?
How we choose the mobile phase for method development.?
What is column in chromatography?
What group of elements were called the inert gases?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
process of Diclofenac sodium,IP.
analytical method validation require to with respect to release specification or shelf life specification?
How do we quantify crystaline and amarpous forms by using (NMR, XRD)spectroscopic techniques? Which any others instruments are useful for this quantification? explain
EXPLAIN THE CALCULATION PART OF AN KF TITRATOR CALIBRATION WITH SUITABLE EXAMPLE
Explain acid gas?
why using HCLO4 in potentiometry?. what are the chacterestics of HCLO4.
Principle of single pan analytical balance