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what is procedure of actual procedure for registration of drug?
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why we use only sucrose in the calibration of polarimeter?
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which situation gc hs and gc als require to use?
For standardization of volumetric solutions, acceptance limit for concentration is considered as 10% of nominal concentration and %RSD as NMT 0.2% (for appropriate no. of replicates). But , if %RSD has not met, what should be further action?
why we use TLC?
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How can the GC or HPLC method is selected to determine the impurity profile in drug product?
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Describe your experience with analytical instrumentation?
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what is a placebo peak
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why we use polystyrene film for ftir calibration?
How to determine retention time in Chromatography
Organic Chemistry 
