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Research and Practice on Non-clinical Safety Evaluation Techniques for Innovative Biomaterials
【Abstract】
1. The Development of Innovative Medical Devices under Regulatory Science
2. How to Conduct Non-clinical Safety Evaluation of Innovative Medical Devices
3. Research and Practice on Evaluation Techniques for New Medical Devices
【Bio】
Liang Jie is a professor at the School of Biomedical Engineering, Sichuan University and the National Engineering Research Center for Biomedical Materials. She is also a doctoral supervisor. In addition, she serves as the vice president of the Institute of Medical Device Regulatory Science, Sichuan University and the director of Sichuan Testing Center for Biomaterials and Medical Device. Her main research focuses on the testing and evaluation technologies and methodologies of biomaterials and medical devices. Her major academic positions include council member of the Chinese Society for Biomaterials and deputy director of the Regenerative Medicine Materials Branch, standing committee member of the Tissue Regeneration Branch of the China Association for Medical Equipment, deputy director of the National Technical Committee for Biological Evaluation of Medical Devices (SAC/TC248), member of the National Technical Committee for Standardization of Dental Materials and Dental Instruments (SAC/TC99), member of the National Technical Committee for Standardization of Surgical Implants and Orthopedic Devices (SAC/TC110/SC3), member of the Professional Technical Committee for Classification and Definition of Medical Devices of the National Medical Products Administration, and external expert of the Medical Device Technical Evaluation Center of the National Medical Products Administration.
TCT Asia
