Answer Posted / mohit thummar
*Q is the amount of dissolved active ingredient specified in the individual
monograph, expressed as a percentage of the labeled content.
| Is This Answer Correct ? | 5 Yes | 0 No |
Post New Answer View All Answers
What is Band broading effect explain
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
WHAT IS THE PURPOSE WE USE HCL, CHOPPER, BURNER, MONOCHROMATOR in AAS? PLEASE EXPLAIN BRIEFLY
what you do when compound having dwel wavelength?
How do we fix the sample concentaryion in hplc method development?
in api coa contains only process impurities and in product coa contains degradation impurities?
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
which are the diffrent batches in the pharmaceuticals?
What is mean by PDR?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
WHY given much noise PDA dector then VWD Dector
why multimedia dissolution require to do?
what is diffrence between specificity and selecivity?
how you confirm the assay method?
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.?
