讯:
中印论坛:从医药大国到医药强国
第三届中印论坛将围绕如何从医药大国到医药强国的主题,针对中国制药的现状,在仿制药行业的政策法规及仿制药领域的热点、疑点展开一系列的对话,嘉宾来自中印两国医药领域相关的政府部门、行业协会及富有经验的领军企业。现场实时对话,帮您答疑解惑。请您提前预定坐席。
主办单位:中国化学制药工业协会
印度制药商协会
国药励展
会议时间:
会议地点:厦门国际会展中心 305会议室
会议内容:
★ 9:20-9:30 协会嘉宾致欢迎辞
★9:30-10:30 仿制药的监督管理及相关问题
SFDA政策法规司相关负责人
内容简介:
针对仿制药监管领域的问题与热点,进行说明。
Mr.Daara Patel 印度制药商协会秘书长
内容简介:
带您了解世界仿制药的最新资讯,印度仿制药领域的发展与现状。作为印度药品制造商协会,其会员750余家企业,成药产品占印度市场的75%,其权威、详实的报道将对行业发展有深远地影响。
★ 13:30-14:30 创建外向型医药企业
海正药业 副总 朱康秦
内容简介:
结合海正国际化遇到的问题与成果,分享海正多年发展外向型企业的经验。
★ 14:30-15:30 CGMP指导下的质量控制体系
Mr. S. M. Mudda,印度 MICRO LABS 公司执行总监
内容简介:
他山之石可以攻玉,Mr. S. M Mudda 在制药领域35年,对怎样进入国际市场,如何进行产品注册,怎样贯彻质量控制体系有着专业的见解。本次论坛以质量控制体系为基础,将带您一同了解印度企业的国际化过程。这将对国内企业如何参与国际市场竞争有着广泛的借鉴意义。
★ 15:30-17:00 问答
The Third Sino-India Forum focusing on how to turn a pharmaceutical power from major to strong. Leading speakers from SFDA, association and famous companies will deliver topics regarding regulatory affairs & generics, bring you the industry knowledge for both countries and open the gate to
Organizers:
Indian Drug Manufactures' Association (IDMA)
Reed Sinopharm Exhibitions Co., Ltd.
Time: 9:20–17:00, Nov. 8th, 2012
Venue: Room 305, Xiamen International Conference & Exhibition Center
Contents:
★ 9:20-9:30
Address by CPIA & IDMA
★9:30-10:30
The regulatory affairs of China Pharmaceutical Industry
Officer of Dept of Policy and Regulations of SFDA
Focus on the generic drugs supervision of hot points, special questions.
★ 10:30-11:30
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Mr Daara Patel Secretary General, IDMA
Bring the latest knowledge of the world generic industry, the development and current situation of Indian industry. More than 750 enterprises, take 75% of the entire
The authentic report will effect the further development of the whole pharma industry.
Highlighting the global need for affordable quality generics from
★ 13:30-14:30
How to establish export-oriented enterprises
VP Zhu Kangqin Hisun Pharmaceutcial
Based on the trouble and achievement of Hisun Pharmaceutical's internationalization, share the passed experiences to establish export-oriented enterprise.
★ 14:30-15:30 CGMP
Quality systems approach for CGMP implementation
Mr. S. M Mudda, Executive Director-Technical & Operations, MICRO LABS LTD.,
35 years' rich experience will tell you how to create quality manufacturing system for achieving current GMP standards
★ 15:30-17:00 Panel discussion.