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王伟光
    男,汉族,1950年2月出生,山东海阳人。1967年11月参加工作,1972年11月加入中国共产党,博士研究生学... 详情>>
李 扬
    1951年9月出生,籍贯安徽,1981年、1984年、1989年分别于安徽大学、复旦大学、中国人民大学获经济学学... 详情>>
李培林
    男,山东济南人。博士,研究员,中国社会科学院副院长,中国社会学会副会长,中国社会科学院社会学研究所副所长。《社会... 详情>>

    中国药品安全与监管政策研究报告

    摘要

    2012年,我国多项医药卫生“十二五”专项规划陆续颁布,指导着医药产业发展方式转变和药品质量提升的监管工作;医药工业组织结构调整成效显著,商业组织结构调整缓慢,创新药物研发成果显著,药品安全保障能力明显提高。基于对我国医药产业发展状况、“十二五”专项规划、药品监管政策、药品安全形势的深入分析,研判“十二五”期间会推进药品上市后再评价、促进企业提升管理水平、加强药品监管国际化合作、提高监管专业化和技术化水平,构建安全责任体系和强化医药企业社会责任的政策趋势。 <<
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    Abstract

    In 2012, China issued the healthcare programs of the "12th Five-year Plan" in succession, providing the guidance for regulating change of the economic development mode of the medical industry and improvement of the drug quality;and pharmaceutical companies made the effective structural adjustment while the distributors proceeded slowly in structural adjustment, the exciting results were obtained in the innovative drug research and development, and the ability for ensuring drug safety has been improved significantly. We made the detailed analysis on the development condition of the medical industry in China, the medical "12th Five-year Plan", the drug regulatory policies and the condition of drug safety;and proposed to perform the quality conformity of generic drugs, promote the new GMP certification, enhance the international cooperation in drug regulation, improve the professional and technical level of regulations, and conduct and encourage the regular special rectifications and the industrial self-discipline management of companies during the "12th Five-year Plan". <<
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    作者简介
    上海市食品药品安全研究中心课题组:课题研究总负责:唐民皓;审核:顾振华、高惠君;执笔人:丁冬、高磊、李伟
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