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2012年中国生物药峰会

生物药,生物仿制药,注册法规,美国药监局,中国药监局,欧洲药品评价局,生物药药企,原研药药企,生物药,生物技术公司,研发外包,生产外包,实验室分析,质量管理,生物药质量控制,生物药非规范性市场,生物药专利,多靶点设计,生物等效性,生物可比性,中试放大,发酵罐,单克隆抗体

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2012年中国生物药峰会 | nextbio-china.com Reviews
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生物药,生物仿制药,注册法规,美国药监局,中国药监局,欧洲药品评价局,生物药药企,原研药药企,生物药,生物技术公司,研发外包,生产外包,实验室分析,质量管理,生物药质量控制,生物药非规范性市场,生物药专利,多靶点设计,生物等效性,生物可比性,中试放大,发酵罐,单克隆抗体
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加入您的日程表,english,注册参会,会议日程,赞助机会,关于峰会,会议背景,参会价格,资料下载,合作媒体,电子快讯,交通住宿,cphi中国会议系列,中国仿制药峰会,cphi医药中国峰会,新型给药系统峰会,联系我们,了解区域性法律法规更新,选择高利润市场与品种,优化技术与开发策略,生物药将成为新一轮的利润增长点吗,生物药最新市场动态,中国药监局已经启动制定 生物仿制药,全球进入临床试验的 生物药,中,将有30%最终成功进入市场销售,这一比率远高于传统的化学药或小分子化合物,日 相聚上海,点击这里
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2012年中国生物药峰会 | nextbio-china.com Reviews

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生物药,生物仿制药,注册法规,美国药监局,中国药监局,欧洲药品评价局,生物药药企,原研药药企,生物药,生物技术公司,研发外包,生产外包,实验室分析,质量管理,生物药质量控制,生物药非规范性市场,生物药专利,多靶点设计,生物等效性,生物可比性,中试放大,发酵罐,单克隆抗体

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