In pharmacopeal solibility parameter of a material, is et
essential to test all paramete? If 70-75% parameter passes
can we assess that the material is satisfactory or not?
Difference between the quantitative analysis and qualitative analysis?
what is procedure of actual procedure for registration of drug?
What is the difference between known and unknown impurities?
why should we do limit of stray light in UV calibration and why should use potassium chloride
why we use actone for Gpv test in hplc calibration
what king of work is done in Regulatory Affairs in Pharma industry ?
Why we are using only KBr in IR spectrometer why not KCl
in hplc calibration we are using 0.05% acetone why we are using that one and what happen when its conc increases or decreases
4 Answers Aurobindo, Cadila, Martin,
How can I develope method of dissolution by HPLC OR UV
why we are use metthanol variously in kfr?why don't use other solutions?
is there any material other than caffene to calibrate hplc detector
what is mean by 40 in the dissolution basket mesh size?