Workshops

Orphan Drugs: SFDA's initiatives and International Experience in Orphan Drug Regulations and Postmarketing safety of Orphan Drugs

Product Verification and Validation Requirements for Medical Devices

Antimicrobial Resistance (AMR) from Food Safety Awareness perspective

Population Pharmacokinetics. Simulation and Moodelling

Clinical Evaluation and Post Market Clinical Follow-up

Overview on the new SFDA IT service "Overseas Medical Devices Manufacturer Account"

Saudi Unique Device Identification (SAUDI-DI) for Medical Devices Requirements & Submission Process

Product Sterilization Requirements for Medical Devices

Clinical Evaluation and Post Market Clinical Follow-up