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中国药品批准改革制度:高级圆桌会议

By Slator

Jul 12

| Pudong, China

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中国监管环境正在快速地发展。2015年8月,国务院发布了《关于改革药品审评审批制度的意见》。仅仅几个月后,2015年11月,中国食品药品监督管理局随后发布了关于药品注册审评审批制度几大政策的通告。

改革致力于使审评制度更加有效,在2016年底之前消除未办理的药品申请。

请加入15位高级专业人士团队,可以学习到最近改革对于临床研究组织和制药企业的日常运营的影响。

此次互动圆桌研讨会将在中国上海浦东香格里拉大酒店11:30 – 14:00进行。

演讲者吕超在上海食品药品监督管理局供职超过11年,主要从事药品、医疗器械、食品、保健食品、化妆品研发、生产、经营、使用等各环节的监管工作。

现供职于环球律师事务所,从事医药健康领域的专业法律咨询,包括合规,争议解决等。

与会者

●      Head of Operations
●      Clinical Operations Director
●      Head of Clinical Operations
●      Head of Regulatory Affairs
●      Clinical Study Manager
●      Publication Manager

此次高级圆桌会议是由Lionbridge(莱博智)全程赞助,Lionbridge(莱博智)是全球最大的为医药,医疗设备及CRO企业提供语言服务服务商。

Screen Shot 2015-10-15 at 11.08.51 AM

 

 

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