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Aid conditionalities international Good Manufacturing Practice standards and local production rights: a case study of local production in Nepal

机译:援助条件国际良好生产规范标准和本地生产权:尼泊尔本地生产的案例研究

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摘要

BackgroundLocal pharmaceutical production has been endorsed by the WHO as a means of addressing health priorities of developing countries. However, local producers of essential medicines must comply with international pharmaceutical standards in order to be eligible to compete in donor tenders. These standards determine production rights for on-patent and off-patent medicines, and guide international procurement of medicines. We reviewed the literature on the impact of Good Manufacturing Practice (GMP) on local production; a gap analysis from the literature review indicated a need for further research. Over sixty interviews were conducted with people involved in the Nepali pharmaceutical production and distribution chain from 2006 to 2009 on the GMP areas of relevance: regulatory capacity, staffing, funding and training, resourcing of GMP, inspectors’ interpretation of the rules and compliance.
机译:背景技术世卫组织已批准本地药品生产,以解决发展中国家的卫生优先事项。但是,当地的基本药物生产商必须符合国际制药标准,才能有资格参加捐助者招标。这些标准确定了在专利和非专利药品的生产权,并指导药品的国际采购。我们回顾了有关良好生产规范(GMP)对本地生产的影响的文献;文献综述的差距分析表明需要进一步的研究。 2006年至2009年期间,与尼泊尔药品生产和分销链有关的人员就GMP的相关领域进行了六十多次访谈,包括监管能力,人员配备,资金和培训,GMP的资源配置,检查员对规则的解释和遵守情况。

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