俄罗斯市场药品质量问题(1992-2004)。报告二世。对新的和连续生产的药物的控制]。

Q4 Medicine
V G Ignatiev, S N Zatravkin, E A Vishlenkova
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引用次数: 0

摘要

俄罗斯卫生部的档案、期刊出版物、访谈和回忆录证明,1992-2004年期间,药品质量问题是俄罗斯制药公司生活中的关键问题。对药物安全的支持不仅被视为社会政策的一部分,而且被视为可用于将“野集市”改造为“受控市场”的规则。媒体纠纷、部门辩护、政治法案和回忆录让我们了解“问题的代价”(情绪高涨、野心勃勃、经济损失)。此外,取决于谁来决定质量(从而评估制药市场的所有参与者)取决于市场权力中心的位置。该研究的作者在一系列报告中介绍了建筑材料,建筑师和俄罗斯控制和授权系统和市场规则的建筑技术的历史重建结果。本报告涉及新的和连续生产的药物的专业知识的做法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The problem of quality of medications at Russian market (1992-2004). Report II. The control of new and serially produced medications].

The archives of the Ministry of Health Care of Russia, journal publications, interviews and memoirs testify that issue of medications quality was key issue in life of Russian Pharma in 1992-2004. The support of medication safety considered not only as part of social policy, but also as rules that could be used to reformat the "wild bazaar" into "controlled market". The media disputes, departmental justifications, political bills and memoirs give idea about "price of the issue" (heat of emotions, ambitions, financial losses). Besides, depending on who would determine quality (and thus to evaluate all players of Pharma market) depended placement of center of power in market. The authors of the study present in series of reports results of historical reconstruction of building materials, architects and technologies of construction of Russian control and authorization-based system and market rules. This report deals with practices of expertise of new and serially produced medications.

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来源期刊
CiteScore
0.40
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