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.?
276what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
324What is the formula for relative diffrence for standard solution in solution stability in validation?
291[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
297in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
333If 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
341Post New Analytical Chemistry Questions
In which situation we require to prepare the standard solution from sample in Related substance method?
how decide the clining method and cleaning method validation require for this perticular products?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
How do we fix the sample concentaryion in hplc method development. What is the basis?
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 the main difference between ODS1 and ODS2 Hplc column.
What is aggregate and fragments in SEC?
What is column in chromatography?
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 can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
what is mean by dissolution hydrodynamics?
