Workshops

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

The Requirements for Biological Evaluation and Biocompatibility of Medical Devices

Requirements of Clinical Evaluation and Post Market Clinical Follow-up

Product Verification and Validation Requirements for Medical Devices

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