Forum Agenda
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Keynote Forum: The Global Journey of China’s Innovation Drugs
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Future-Driven Intelligent R&D–AI for Life Sciences and Drug Discovery
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The Era of Superintelligent Agents for Chinese Innovative Drugs
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Panel Discussion: AI-Empowered Four-in-One Translation Platform
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AI-Driven Innovation Practices in Pharmaceutical Enterprises
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AI·Intelligent Transformation: From Data Foundation to Scenario Value
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Medicine-Engineering Integration and Innovative Medical Devices
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Cross-Border Cooperation and China’s New Drug Global Expansion
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Global Development of Pharma Enterprises and Emerging Market Cooperation
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China-Japan Cooperation Session: Leveraging Japan’s Market to Boost Overseas Expansion Strategies
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Legal Safeguard and Value Empowerment for Globalization of Chinese Pharma Enterprises
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Clinical Development of Next-Generation Innovative Oncology Drugs
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Global BD Cooperation Session for Innovative Drugs – Track 1, 2 & 3
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Collaboration Between North American and Chinese Innovative Drug Industries
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Biosimilars Commercialization & Global Launch Session(China Focus)
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Protheragen Session: Global Biomedical Cross-Border Transactions
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Clinical Development of Next-Generation Innovative Oncology Drugs
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U.S. Biotech Tensions and the Future Road for Chinese Pharmaceutical Companies Going Global Session
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July 23,09:00-12:10
Decree No. 818 and a New Era for the Development of Biomedicine Industry session
Stay tuned
Conference Planning
Jie Li,Senior Vice President, Regulatory Affairs, Aeira Health; Director, All-Chain Pharmaceutical Information Research Institute, Beijing Economic-Technological Development Area
moderator
Jinsheng Cheng,General Manager, Life Science Division, Tofflon
09:00-09:20 Interpreting Decree No. 818
Jianzhong Shen:Coordination Commissioner for the Implementation of Regulation 818 of the Biology Center, Second-Class Researcher (Former Deputy Director)
09:20-09:35 Decree No. 818 and the Boao Lecheng Pilot Zone
Jingle Liao:Deputy Director of the Hainan Boao Lecheng International Medical Tourism Pilot Zone Administration
09:35-09:50 Cell Therapy-Based Cancer Vaccines: Translational Practice Under Decree No. 818
Genhong Cheng:Fellow of the American Academy of Microbiology,Tenured Professor at UCLA,Distinguished Professor, Guangzhou Laboratory
09:50-10:05 New Biomedical Technologies in the Era of Decree No. 818
Biao Wu:Deputy Director, Changzhou West Taihu Institute of Advanced Cell Therapy Technology; Vice Chairman, China Medicinal Biotech Association
10:05-10:20 Building an End-to-End Support System for Decree No. 818: The West China Hospital Approach
Yuan Li:Deputy Director of the Department of Science and Technology and Director of the Research Platform Management Office, West China Hospital of Sichuan University
10:20-10:40 Tea break
10:40-10:55 Managing Somatic Cell Clinical Research Under Decree No. 818: The SYSUCC Experience and Practices
Tong Xiang,Associate Research Fellow, Experimental Research Department, Sun Yat-sen University Cancer Center
10:55-11:10 The Role of Ethics in Reviewing New Biomedical Technologies Under Decree No. 818
Jie Li:Director, Ethics Committee, Peking University Cancer Hospital
11:10-11:25 A Brief Analysis of CGT Product R&D Pathway Strategies and Prospects Under the 818/828 Policies
Zhihong Wan:Chief Scientist & New Drug Evaluation Expert, Boji Medical
11:25-12:10 Roundtable: Operationalizing Translational Biomedical Technologies Under the 818 Policy
Jie Li:Senior Vice President, Regulatory Affairs, Aeira Health; Director, All-Chain Pharmaceutical Information Research Institute, Beijing Economic-Technological Development Area
Guodong Jia:Distinguished Research Fellow, Nanhu Laboratory
Hongxin Deng:Professor, National Key Laboratory of Biotherapy, West China Hospital, Sichuan University
Xueli Geng:Executive General Manager, SDIC Venture Capital
Jinsheng Cheng:General Manager, Life Science Division, Tofflon
Mingyu Liu :Head of R&D and TIL Program Leader, Biosyngen