Workshops

Requirements for Points of Care (POC) Medical Devices Manufacturing

Contact lenses and solutions technical Requirements

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

Introducing the rules for classifying the risk of medical devices

Additional Risk Minimization Measures : Overview and Local and International experience in Measuring Their Effectiveness

Requirements for Clinical Trials of Medical Devices

SFDA workshop on quality variation in pharmaceutical products (Requirements and conditions)

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

Risk Management for Medical Devices: ISO 14971 Requirements