Pharma Products Registration in Saudi Arabia – Complete SFDA Guide (2025)
Saudi Arabia’s pharmaceutical market is expanding rapidly, but entry requires strict compliance with the Saudi Food and Drug Authority (SFDA). From appointing a local representative to preparing a Common Technical Document (CTD), securing GMP approvals, and meeting labeling standards, the registration process ensures safety, quality, and legal compliance. This guide outlines the step-by-step process, required documents, timelines, and compliance essentials for smooth market entry.