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中国药学(英文版) ›› 2014, Vol. 23 ›› Issue (1): 69-70.

• 【 其 它 】 • 上一篇    

第二届中国医药发展论坛暨药品质量与市场准入研讨会召开

北京大学药学院 药事管理与临床药学系   

  1. 北京大学药学院 药事管理与临床药学系
  • 收稿日期:2014-01-05 修回日期:2014-01-15 出版日期:2014-01-23 发布日期:2014-01-22
  • 通讯作者: 北京大学药学院 药事管理与临床药学系

The 2nd “China Medical Development Forum”, A.K.A. the Seminar of Drug Quality and Market Access

Department of Pharmacy Administration and Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China   

  1. Department of Pharmacy Administration and Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
  • Received:2014-01-05 Revised:2014-01-15 Online:2014-01-23 Published:2014-01-22
  • Contact: Department of Pharmacy Administration and Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China

摘要:

20131227,北京大学医药管理国际研究中心和北京大学医药研究发展中心联合主办的第二届中国医药发展论坛暨药品质量与市场准入研讨会在北京大学医学部逸夫楼报告厅隆重召开。原国家食品药品监督管理局局长邵明立,北京大学常务副校长、医学部常务副主任柯杨,相关政府部门管理人员、高校专家学者、医院药房临床药师,以及医学部领导、药学院负责人和研究中心的专家教授出席论坛。
柯杨教授首先代表学校发表讲话。她指出,药品质量与市场准入这一选题和我国当前医药卫生体制改革、医疗模式改变具有深刻的联系,专家学者们专业力量的注入,将成为整个药品安全改革中的重要力量。她强调,药品质量源于设计的理念决定了药品安全涉及众多环节,越来越多的实践证明学科交叉、自然科学和社会科学结合才能真正的解决医疗问题、医疗体制问题和人类健康问题。她希望将论坛坚持办好、办长久。邵明立代表中心学术顾问讲话。他肯定了研究中心多年来秉承确保公众用药安全、有效、合理,推动医药产业健康发展的宗旨做出的努力和发挥的功效,感谢北京大学、医学部等各方面对研究中心的支持。他强调,党的十八届三中全会首次把药品安全纳入公共安全体系建设,这是对“药学人”提出的更高要求。他期望药品安全领域专家针对重大理念的发展,能够取得更多更好的成果。
      …………

Abstract:

      In December 27, 2013, the 2nd “China Medical Development Forum”, A.K.A. the Seminar of Drug Quality and Market Access, jointly managed by Peking University International Research Center of Medicinal Administration(IRCMA) and Center for Research and Development of Medications (CRDM) was ceremoniously held in Peking University Health Science Center (PHUSC). Prof. Mingli Shao, the original director of State Food and Drug Administration (SFDA) and Prof. Yang Ke, associated president of university, government managers, university scholars, hospital pharmacists, and experts of IRCMA and CRDM attended the forum. 
      At the start of the forum, Prof. Yang Ke delivered a speech on behalf of PHUSC. She pointed out that drug quality and market access have a close contact with healthcare reform, experts and scholars’ participation will contribute a lot to the reform of drug safety. She emphasized that the quality of drug depended on the quality of design, which made drug safety related to multiple steps, more and more practice proved that multidiscipline and a combination of natural and social sciences could indeed solve problems related to medical, healthcare system, and human health. Finally, she put forward the hope of long-term development of the forum. Prof. Mingli Shao also delivered a speech representing academic advisers of IRCMA, highly praised the efforts and achievements the IRCMA had made on ensuring drug safety, rational use of medications, and promoting the healthy development of pharmaceutical industry. He thanked the support from PUHSC to IRCMA. 

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