Basic principle of ESI?
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If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
how do u optimise hplc method
HPLC Calibration was done in Reverse Phase, but not in normal phase why explain?
what is mean by Q in S1 and S2
What is difference between oos
(0.41)d what is d?
How is the Flame test performed?
how do you established the RRF for unknown impurity
why reference flow required during hplc analysis on rid?
in which situation require to change rs specification?
why there is a need of optical activity & specific optical activity measurement by polarimeter
difference between precision & accuracy.