Workshops

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

Clinical Trials of Medical Device Requirements

Medical Devices Marketing Authorization (MDMA) Requirements for contact lenses and contact lenses Solutions

Risk Management for Medical Devices: ISO 14971 Requirements

Product Verification and Validation Requirements for Medical Devices