我国药用辅料监管体制研究
发布时间:2018-05-26 23:01
本文选题:药用辅料 + 监管模式 ; 参考:《云南大学》2012年硕士论文
【摘要】:药用辅料涉及公民生命安全及身体健康,也涉及整个国家和社会的治安。因此,作为一个社会问题,药用辅料的监管成为全社会关注的对象。在我国改革开放后,药用辅料监管开始进入起步期。科学技术的进步和社会的发展带给人们物质基础极大满足的同时也成为社会的安全隐患,仅依赖市场调节已经远远不能满足公民对药用辅料质量安全的需求。频发的药用辅料质量安全事故使全社会消费者对此产生了疑虑,也严重影响公众中心目中的政府形象。 如何对药用辅料监管合理运用,成为药用辅料高效运行的前提。我国药用辅料质量安全越来越受人们关注,我国对此已做了一些监管模式方面的改善,并采取了一定的程序和相关措施。但是,药用辅料的质量安全形势在我国依然不容乐观。 本文从理论研究的基础上,根据我国药用辅料监管定义、发展和现状开始分析,通过对理论分析,依据外国的先进管理经验,结合我国实际情况,试探寻药用辅料监管的内因和外因,同时分析目前我国药用辅料监管中存在的原因及问题,提出了我国药用辅料监管体制的建议。全文共分为五个部分。
[Abstract]:Medical excipients are related to the safety and health of citizens and the public order of the whole country and society. Therefore, as a social problem, the supervision of pharmaceutical excipients has become the focus of the whole society. After the reform and opening up in China, the supervision of pharmaceutical excipients began to enter the initial stage. The progress of science and technology and the development of society bring great satisfaction to people's material base, but also become the hidden danger of social safety. Relying on the market regulation is far from satisfying the citizens' demand for the quality and safety of medical excipients. The frequent accidents of quality and safety of medical excipients make the whole society have doubts about this, and also seriously affect the government image in the eyes of the public. How to supervise the rational use of pharmaceutical excipients has become the premise of efficient operation of pharmaceutical excipients. More and more attention has been paid to the quality and safety of pharmaceutical excipients in China. However, the quality and safety situation of medicinal excipients is still not optimistic in China. On the basis of theoretical research, according to the definition, development and current situation of the supervision of pharmaceutical excipients in China, this paper begins to analyze the theoretical analysis, according to the advanced management experience of foreign countries, combined with the actual situation of our country. This paper probes into the internal and external causes of the supervision of pharmaceutical excipients, analyzes the causes and problems existing in the supervision of pharmaceutical excipients in China, and puts forward some suggestions for the supervision system of pharmaceutical excipients in China. The full text is divided into five parts.
【学位授予单位】:云南大学
【学位级别】:硕士
【学位授予年份】:2012
【分类号】:F203
【引证文献】
相关期刊论文 前1条
1 傅议娇;单友亮;鲁艺;;对药用辅料监管现状的几点思考[J];中国药事;2013年10期
,本文编号:1939281
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