How to compare XRD graphs against standard and carry polymorpism study of API's by powder XRD method?
if rsd failed then what require to do?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
in dissolution why pool sample needed? in which type of drug pool sample need?
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?
Principle of single pan analytical balance
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
which are the sizes of capsules?
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
if you given one product then which tests you will perform?
In Dissolution Test why limit is define Q+5% what is the role of +5%.
We use Potassium Dichromate solution for the calibration of UV-Visible Spectrophotometer in UV region. My question is to calibrate visible region which solution could be used in photometric accuracy
what is biorelivent dissolution media?
why we use a particular hplc column for a particular compound give reasons?please