Workshops

Artificial Intelligence and Software Based on Medical Devices

Introduction to Biological evaluation for Medical Devices

The Requirements of Clinical Evaluation Report (CER)

Clinical Trials of Medical Device Requirements

Product Verification and Validation Requirements for Medical Devices

Risk Management for Medical Devices: ISO 14971 Requirements

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

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

Biotechnology and Innovation in Medical Devices industry