ANALYTICAL QUALITY BY DESIGN-DRIVEN DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RP-UPLC METHOD FOR SIMULTANEOUS DETERMINATION OF DULOXETINE HYDROCHLORIDE AND PREGABALIN IN BULK AND PHARMACEUTICAL DOSAGE FORM
Objective: The present study aimed to validate and develop a robust, stability-indicating Reversed Phase-Ultra Performance Liquid Chromatography (RP-UPLC) method for the concurrent determination of Pregabalin and Duloxetine Hydrochloride using the Analytical Quality by Design (AQbD) Principles. Methods: An AQbD-assiste...