Workshops

Regulatory Considerations and Localization of CAR T-Cell Therapy

Risk Management for Medical Devices: ISO 14971 Requirements

Introducing the rules for classifying the risk of medical devices

API Quality Assessment for Generic Products

Safe Handling and Disposal of Hazardous Medications

Medical Devices Marketing Authorization (MDMA) Requirements for Contact lenses and Contact lenses solutions

Introduction to Medical Devices Quality Management System ISO 13485

Novel Food and Feed at SFDA - Supporting Research and Innovation

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