If calibration of 12 bowl dissolution apparatus does not
meets single stage procedure, how can you precede calibration?
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If we get 100% assay of an Initial sample ,and the stability studies of the same sample got 90% dissolution result, and when the same stability sample was analyzed for RS studies no impurities was found . Where the 10% Active substance were gone during dissolution analysis.Please help me in getting the conclusion.
Why 3X sampling plan are implemented in process validation?
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0 Answers Abbott, Cipla, Ranbaxy,
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What is difference between assay and content uniformity ?
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