Development and Validation of UPLC Method For Simultaneous Quantification of Carvedilol and Ivabradine in The Presence of Degradation Products Using DoE Concept
Quality-by-design-based development and validation of a stability-indicating UPLC method for quantification of teriflunomide in the presence of degradation products and its application to invitro dissolution
Supercritical Fluid (CO2) Chromatography For Quantitative Determination of Selected Cancer Therapeutic Drugs in The Prescence of Potential Impurities in Injection Formulations