Answer / ameer

http://www.usp.org/sites/default/files/usp_pdf/EN/USPNF/pharmaceuticalDosageForms.pdf

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.

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