For Recent draft guidelines for Dissolution test apparatus
calibration, why removing the salicylate tables?
Answer Posted / k l srinivas
due to major variations are coming
|Is This Answer Correct ?||1 Yes||3 No|
which are the diffrent batches in the pharmaceuticals?
if you have given a blank water how you analyse by general analytical techniques?
what you do when compound having dwel wavelength?
Why six unit used for precision?
in dissolution why pool sample needed? in which type of drug pool sample need?
In rs method development when we are going area normalization method to dilute standard method?
How we can identify process related and degradation impurity in single method with short period?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
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 you fix the limits of impurities?
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
iam usig ph buffers merk. manually how to prepare ?
What is split ratio in Gc? Splitless? how requirr to select?
What is column in chromatography?