how you start RS method development when for new product?

how you establish the LOQ?

in which situation require to use paddle and basket?

what is mean by dissolution hydrodynamics?

column washing procedure for normal phase and reverse phase?

how to convert normal phase hplc to reverse phase and vice versa?

if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?

what is mean by extactable and leachable study?

how to calculate elemental impurities?

how you fix the limits of impurities?

what is mean by nitrosamine impurities?

if instrument calibration fails then what require to do?

why require the ph, buffer during hplc mobile phase?

is it nessesary to do solution stability for 7 days?

which are the diffrent batches in the pharmaceuticals?