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Answer Posted / haresh c prajapati
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in api coa contains only process impurities and in product coa contains degradation impurities?
what is mean by covalidation
how require to interprit the method precision data of hptlc?
what is definition of validation? which components are followed give detail?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
EXPLAIN THE CALCULATION PART OF AN KF TITRATOR CALIBRATION WITH SUITABLE EXAMPLE
which are the diffrent batches in the pharmaceuticals?
How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
If combination product how require to identify which imp is of which api?
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?
what is mean by nitrosamine impurities?
if you have given a blank water how you analyse by general analytical techniques?
What is the main difference between ODS1 and ODS2 Hplc column.
how to select short coloum and long coloumn for new molecule
