European Chamber 1st Medical Device Forum 中国欧盟商会第一届医疗器械论坛 Go back »
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Time2019-12-18 | 09:00 - 17:00
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Venue:Infinity Ballroom, First Floor, Hilton Beijing | 北京希尔顿酒店一层 天元宫
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Address:
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Fee:Members: 880 |
Non Members: 1280
医疗改革一直是中国改革进程的首要议题。医疗器械在预防、诊断和治疗疾病方面发挥着至关重要的作用。《“健康中国2030”规划纲要》提出改善人民健康水平的目标,而医疗器械正是实现这一目标的关键。
Refining the healthcare system has always been a priority for China during the country’s reform process. As medical devices play a crucial role in the prevention, diagnosis, and treatment of diseases, this makes the products key to the goal of improving the overall health of the population, laid down in the government’s strategic plan Healthy China 2030.
为促进产业发展、三医联动,中国欧盟商会协同COCIR定于2019年12月18日在北京希尔顿酒店,举办第一届医疗器械论坛。本届会议主题为“医疗器械监管、产业创新和发展,助力健康中国”。
Therefore, the European Chamber is delighted to hold its First Medical Device Forum, co-hosted by COCIR, at the Hilton Hotel in Beijing, on 18th December 2019. The theme is ‘Enhancing Healthy China: Medical Device Supervision and Innovation and Development of the Industry’.
本次会议语言为中文,会提供同传设备。
The event will be in Chinese with simultaneous Chines -English translation.
拟定会议议程 Tentative Agenda
08:30-09:00 签到注册 Registration
09:00-09:10 中国欧盟商会秘书长致欢迎辞 Welcome Remarks by Secretary General, European Chamber
09:10-09:20 欧盟驻华代表团贸易处一等参赞致开幕辞 Opening Remarks by First Counsellor, Trade Section, Delegation of the European Union to China
09:20-09:30 国家药品监督管理局相关领导致开幕辞 Opening Remarks by government official, National Medical Products Administration (NMPA)
主论坛 Plenary
医疗器械监管、产业创新和发展,助力健康中国
Enhancing Healthy China: Medical Device Supervision and Innovation and Development in the Industry
09:30-09:50 国家药品监督管理局医疗器械注册管理司 演讲主题《医疗器械审评审批制度改革进展》 Presentation on Progress in Reform of the Medical Device Review and Approval System by Department Medical Device Registration, NMPA
09:50-10:10 人工智能医疗器械标准化技术归口单位 演讲主题《人工智能医疗器械标准化工作进展》Presentation on Progress in the Standardization of Artificial Intelligence Medical Devices by AI Medical Devices Standardization Technical Committee
10:10-10:30 国家卫生健康委员会医政医管局 演讲主题《推进分级诊疗制度建设》 Presentation on Promoting the Development of a Hierarchical Diagnosis and Treatment System by Department of Medical Administration, National Health Commission
10:30-11:00 茶歇 Coffee Break and Networking
11:00-11:20 海关总署商品检验司 演讲主题《海关相关政策介绍》 Presentation on Relevant Legislative and Administrative Customs Frameworks for Medical Devices by Department of Commodity Inspection, General Administration of Customs
11:20-11:40 北京大学公共卫生学院简伟研副教授 演讲主题《DRGs国际经验》 Presentation on International Experiences with Diagnostic-Related Groups (DRGs) by JIAN Weiyan, Associate Professor, School of Public Health, Peking University
11:40-12:00 上海健康医学院医疗器械监管专业蒋海洪主任 演讲主题《医疗器械注册人制度》 Presentation on Marketing Authorisation Holder (MAH) Regime for Medical Devices by JIANG Haihong, Associate Professor, Dean of Medical Device Supervision Major in Shanghai University of Medicine & Health Science
12:00-14:00 午餐 Lunch Break
14:00-14:30 中国卫生经济学会副会长张振忠教授 演讲主题《DRG试点城市效果分析》 Presentation on Analysis of Outcomes from DRG Pilot Cities by ZHANG Zhenzhong, Professor, Vice President, China Health Economics Association
14:30-15:30 圆桌论坛(一) - 改革浪潮下的医疗器械监管
Session One - Medical Devices Administration under the Wave of Reform
讨论涉及话题 Topics:
• 医疗器械技术审评(国家药品监督管理局医疗器械技术审评中心)
Technical review of medical devices (Center for Medical Device Evaluation, NMPA)
• 医院管理的改革,例如不良事件报告、临床试验管理以及UDI实施后医院管理的各方面变化 (王剑,解放军总医院原医学保障部医务办主任)
Hospital management reform, such as adverse events reporting, clinical trial management, and changes in hospital management after the implementation of UDI (WANG Jian, Former Director-General, Medical Affairs Office, Chinese PLA General Hospital)
• 医疗器械标准 (孙卓惠,COCIR中国 标准化工作组主席)
Medical device standards (SUN Zhuohui, Chair, COCIR China Standardization Focus Group)
• 医疗器械质量管理体系现场核查(董斌哲,迈迪思创(北京)科技发展有限公司联合创始人)
On-site verification of medical device quality management system (Frank Dong, Co-founder of Medical Strong (Beijing) Technology Development Co., Ltd.)
• 企业视角谈医疗器械产业监管及市场准入政策 (尹琦曼,中国欧盟商会医疗器械工作组主席)
Corporations’ views on medical device industry supervision and market access policies (Annie Yin, Chair, Healthcare Equipment Working Group, European Chamber)
15:30-16:00 茶歇 Coffee Break and Networking
16:00-17:00 圆桌论坛(二) - 医疗器械产业政策环境展望:机遇与挑战
Session Two - Opportunities and Challenges of Medical Devices Regulatory Environment
讨论涉及话题Topics:
• 医疗器械监管历程以及变革 (常永亨,原中国食品药品国际交流中心副主任)
The course and reform of medical device administration (CHANG Yongheng, Former Deputy Director-General of China Center for Food and Drug International Exchange)
• 全球合作下的创新格局 (石晟昊,国药资本董事总经理)
Innovation landscape of global collaboration (SHI Shenghao, Managing Director, China Pharmaceutical Capital)
• 欧盟市场准入,如欧盟医疗器械法规(计利方,BSI中国区医疗器械业务负责人)
EU market access, e.g. EU regulations for medical devices (Lane Ji, the Medical Device Director of BSI China)
• 数字医疗 (尹鹏翎,励讯集团中国区数据战略发展官)
Digital health (Maggie Yin, Data Strategy Officer, RELX China)
• 医疗器械知识产权保护(夏海波,上海汉盛律师事务所高级合伙人)
Intellectual property protection for medical device (XIA Haibo, Senior Partner of Shanghai Hansheng Law firm)
Views expressed by invited speakers do not necessarily reflect the opinions or position of the European Union Chamber of Commerce in China.
By Bank transfer. Please find the account information below:
A/C Name: 中国欧盟商会
A/C No.: 7110210182500027543
China CITIC Bank 中信银行京城大厦支行
北京市朝阳区新源南路6号京城大厦
Note/备注:20191218MDF
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