Workshops

Product Sterilization Requirements for Medical Devices

Requirements for Clinical Trials of Medical Devices

Product Verification and Validation Requirements for Medical Devices

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

Clinical Trials of Medical Device Requirements