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what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
before starting analytical method valodation what you checking? and how giving preference to start validation?
What is diffrence between extractable volume and deliverable volume? Answer pls
How we choose the mobile phase for method development.?
What is a difference between potency and purity?
if peak get problamatic then what require to do?
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
what are risk assement in the analytical qbd?
which situation gc hs and gc als require to use?
what is the origin to prepare standard operating procedure
What are modes of quantification in related substances
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
Which parameters require to do in tech transfer?
which are the diffrent batches in the pharmaceuticals?
