Ahmed Hosny
Ahmed Hosny is a Stability and Methodology expert with over 17 years of experience in pharmaceutical R&D and Quality Control. He currently serves as QC Manager and R&D Deputy Manager (Stability & Methodology) at ATCO Pharma, and as a Course Instructor at PharmaCores. His expertise includes stability studies (accelerated, long-term, in-use, and ongoing), analytical method validation, comparative dissolution, bioequivalence and biowaiver studies, CTD preparation, and EDA regulatory compliance. Ahmed has extensive experience in managing product registration projects, leading cross-functional launch teams, and handling variations for human and veterinary products in alignment with GMP and international quality standards. He brings strong hands-on regulatory and technical knowledge, delivering practical, regulation-focused pharmaceutical training.
Experience
17+ Years
Stability and Methodology Head with extensive R&D and Quality Control experience, possessing profound professional knowledge of CTD, EDA, GMP/GLP, CAPA, Quality, Stability, and Bio-Equivalence requirements.
Industry Background
Pharmaceutical Quality Control and R&D Methodology
Progressed from Quality Control Specialist at SABAA to QC Manager, R&D Deputy Manager, and Pipeline Products Project Manager for both human and veterinary products at ATCO Pharma.
Academic Background
Master's Degree in Quality Management (MQM) and Bachelor's Degree in Pharmaceutical Science
Earned a Master's in Quality Management with an Excellent grade from the Arab Academy for Science, Technology and Maritime Transport (AASTMT) and a Bachelor's in Pharmaceutical Science from October 6 University.
Areas of Contribution
Quality ControlAnalytical Method DevelopmentBioequivalenceFormulation Development
