Answer Posted / satish
question is wrong 5 mg of sample is neutralized with 1 ml of kf reagent
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pharma industries oriented
Difference between the quantitative analysis and qualitative analysis?
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
Which are the diffrent grades of api in pharma?
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?
what is mean by extactable and leachable study?
how to set sample and standard concentration in RS method?
why we are using benzene, anyline in acetic anhdride assay titration method?
What is shaking level in GC?
how to select short coloum and long coloumn for new molecule
What is diffrence between extractable volume and deliverable volume? Answer pls
what you do when compound having dwel wavelength?
what is biorelivent dissolution media?
Why we use potassium dichromate in uv calibration Exact reason behind it??
how we can identify the impurity is coming below loq at transfering site?
