Workshops

Demonstration of the Medical Device Post-Market Surveillance Requirements

Risk Management for Medical Devices: ISO 14971 Requirements

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

Product Sterilization Requirements for Medical Devices

Guidance on Medical Devices Classification

Artificial Intelligence and Software Based on Medical Device

Clinical Trials of Medical Device Requirements

Demonstration of the Medical Device Post-market surveillance Requirements

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