what are all the needs or pre-requisites to perform project on bracketing and matrixing of stability products?
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what is limit of cleaning validation
What is the limit for friability of tablets?
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How to select HPLC column for particular product.
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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.
Disintegration time for soluble tablet
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