Mohamed Khidr Arafa is a senior R&D and Stability expert with over 13 years of experience in pharmaceutical methodology development, stability studies, and regulatory file preparation. He currently serves as Methodology & Stability Section Head at ATCO Pharma and as a Course Instructor at PharmaCores.
He specializes in analytical method development, validation, verification, and transfer (Assay, Dissolution, Impurities), CTD and bioequivalence file preparation, and regulatory compliance aligned with EDA, ICH, FDA, USP, EMA, and WHO requirements. Mohamed has successfully led multiple regulatory audits (including SFDA and other authorities) with zero critical observations, bringing strong leadership, risk management, and quality-driven expertise into his training programs.
