Workshops

Clinical Trials of Medical Device Requirements

Medical Devices Standards Role in Ensuring Patient Safety

Manufacturing medical devices at Points of Care (POC)

Introducing the Rules for Classifying the Risk of Medical Devices

Artificial Intelligence and Software Based on Medical Device

Explain The Essential Principles of Safety and Performance for Medical Devices

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