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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.?
718what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
900What is the formula for relative diffrence for standard solution in solution stability in validation?
813[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
810in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
845If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
865Post New Analytical Chemistry Questions
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
Which parameters require to do in tech transfer?
how much mass should be there in volumetric flask while in preparation of sample for assay?
what is the procedure for cleaning of lenses of hatr accesory of ftir instrument?
we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion
how pda detector works over uv?
Is it nessesary all multimedia dissolution require descriminatory?
how the compound separate in coulunm,explain
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
In BP2013, Loperamid HCl monograph. Assay by titration with 0.1N sodium hydroxide using hydrocloric acid 0.01N and reading the volume added between the 2 points of inflexion. I have a question that if the diluent solvent is ethanol is certainly consumed a amount of volume of titrant, so this volume must be eliminated on the result calculation or not apart from first point which is subtracted above.
how you establish the LOQ?
What is the Formula for coreletion coefficient in plhplc calibration
for inorganic molecules require to do RS, Assay and disso?
