- 1、本文档共49页,可阅读全部内容。
- 2、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。
- 3、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
查看更多
现阶段我国GMP制度有效实施的关键因素研究及其制度设计
摘 要
Abstract
Research of Significant Factor of GMP to Effcetive move and
Its Design of System in Current Stage
GMP system in China has made progress on improving Chinas pharmaceutical corporation management level, to improve drug quality and ensure safety and efficacy of the people. However, the implementation and development of GMP is a long-term task, during its development process still have some problems. This study aims to summarize experience and analysis the problem, and propose the recommendations, to get the reference for next phase of the GMP implementation and development.
Through review and research the history of GMP production, development and improvement of USA and Japan, based on case studies, comparative demonstration of the GMP development and practice of China made a comprehensive and systematic analysis of exposition to dialectical seen in perspective GMP implementation in China has been achieved, summarized the problems, deeply analysis the source of the problem, learn from the practical experience of developed countries, puts forward the new era of China drug GMP implementation and development of recommendations.
In this paper, through method of theory and literature study and action research, by collecting relevant information, review domestic and international GMP development history, analysis of the current status of GMP system management, summarized Chinas pharmaceutical corporation existing problems, base on competence theory, learn from the experiences of advanced countries, the foundation of a collection of the authors own work practices, GMP system put forward to improve new ideas and new methods.
In my opinion, the main factors affecting the implementation of GMP is the pharmaceutical corporations internal staff issues; the Construction of government departments lack of GMP inspectors, GMP system of relevant laws and regulations and technical standards for system imperfections and other reasons. This article applied competence theo
您可能关注的文档
- 玉米胚芽油创业计划书.doc
- 玉米花生大豆棉花大葱性状考察及测产报告.doc
- 玉米籽粒发育关键基因的克隆与功能解析-洛阳会议.ppt
- 玉米育种相关知识.ppt
- 玉米选择题.doc
- 玉米纸筒育苗移栽机械技术与探讨.ppt
- 玉米须口服液中试放大研究开题报告.doc
- 玉米生产与经营趋势研究.ppt
- 玉米须黄酮体外抑菌作用的研究教研项目申报书.doc
- 玉米超高产栽培技术_吉林农大 (PPTminimizer).ppt
- 《GB/T 10810.3-2025眼镜镜片 第3部分:透射比试验方法》.pdf
- 中国国家标准 GB/T 45283.2-2025工业控制系统人机接口组态文件交互 第2部分:基础交互描述.pdf
- 《GB/T 45283.2-2025工业控制系统人机接口组态文件交互 第2部分:基础交互描述》.pdf
- GB/T 45283.2-2025工业控制系统人机接口组态文件交互 第2部分:基础交互描述.pdf
- 中国国家标准 GB/T 10810.3-2025眼镜镜片 第3部分:透射比试验方法.pdf
- GB/T 10810.3-2025眼镜镜片 第3部分:透射比试验方法.pdf
- 《GB/T 27995.1-2025半成品镜片毛坯 第1部分:单焦和多焦》.pdf
- GB/T 27995.1-2025半成品镜片毛坯 第1部分:单焦和多焦.pdf
- 中国国家标准 GB/T 27995.1-2025半成品镜片毛坯 第1部分:单焦和多焦.pdf
- 《GB/T 10810.5-2025眼镜镜片 第5部分:表面耐磨试验方法》.pdf
文档评论(0)