Workshops

Requirements of Clinical Evaluation and Post Market Clinical Follow-up

Non-Interventional (Observational) Studies in Post-Marketed Drugs Safety

Introduction to Medical Device Executive Regulation and Medical Device Requirements Update

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

Medical Devices Marketing Authorization (MDMA) Requirements for contact lenses and contact lenses Solutions

Product Sterilization Requirements for Medical Devices

Demonstration of the Medical Device post market Requirements

Clinical Trials of Medical Device Requirements

Orphan Drugs: SFDA's initiatives and International Experience in Orphan Drug Regulations and Postmarketing safety of Orphan Drugs