what is procedure of actual procedure for registration of drug?


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How can we calculate offset value pH measurment

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What is a difference between potency and purity?

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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

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