Workshops

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"

Hematological Diseases Health Related Outcomes