Browsing by Author Shah, P.

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Issue DateTitleAuthor(s)
2020Related Impurities HPLC Method Development & Validation for drug combinations: Olmesartan Medoxomil, Chlorthalidone & CilnidipineShah, P.; Dhadhuk, B
2022RP-HPLC In-Vitro Dissolution Method Development and Validation for Determination of Olmesartan Medoxomil, Chlorthalidone and Cilnidipine Drug CombinationsShah, P.; Dhaduk, B.
2023Stability indicating LC-MS/MS method and validation of Selexipag impurities and identification of its force degradation productsShah, P.; Hadiyal, S.; Dhaduk, B.