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How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
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What is the procedure for investigation of an OOS (Out of specification) results?
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why we are performing residue on ignition?
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In which situation we require to analytical method validation of excipient?
During Validation study, Recovery is passing at all levels but Linearity is failing. Justify?
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Why sodium hydroxide used for maintain pH of phosphate buffer
which are the diffrent batches in the pharmaceuticals?
why 0.005 M sulphuric acid is used to calbrate spectrophotometer and why caffiene is used for calibrating hplc
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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?
What is Arsenic Test?
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Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
Any molecule is filing for ANDA purpose, what are the dissolution requirements / specifications needed ?
Organic Chemistry 
