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Identifying market risk for substandard and falsified medicines: an analytic framework based on qualitative research in China, Indonesia, Turkey and Romania

机译:确定不合标准和伪造的药物的市场风险:基于中国,印度尼西亚,土耳其和罗马尼亚定性研究的分析框架

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摘要

Introduction: Substandard and falsified medicines undermine health systems. We sought to unravel the political and economic factors which drive the production of these products, and to explain how they reach patients. Methods: We conducted in-depth case studies in China, Indonesia, Turkey and Romania. We reviewed academic papers and press reports (n = 840), developing semi-structured questionnaires. We interviewed regulators, policy-makers, pharmaceutical manufacturers, physicians, pharmacists, patients and academics (n=88). We coded data using NVivo software, and developed an analytic framework to assess national risks for substandard and falsified medicines. We tested the framework against cases reported to the World Health Organization, from countries at all income levels. Results: We found that increasing political commitment to provision of universal health coverage has led to public procurement policies aimed at lowering prices of medical products. In response, legitimate, profit-driven pharmaceutical companies protect their margins by cutting costs, or withdrawing from less profitable markets, while distributors engage in arbitrage. Meanwhile, health providers sometimes protect profits by 'upselling' patients to medicines not covered by insurers. Cost-cutting can undermine quality assurance, leading to substandard or degraded medicines. Other responses contribute to shortages, irrational demand and high prices. All of these provide market opportunities for producers of falsified products; they also push consumers outside of the regular supply chain, providing falsifiers with easy access to customers. The analytic framework capturing these interactions explained cases in most high and middle-income settings; additional factors operate in the poorest countries. Conclusions: Most efforts to secure medicine quality currently focus on product regulation. However, our research suggests market mechanisms are key drivers for poor quality medicines, including where political commitments to universal health coverage are under-resourced. We have developed a framework to guide country-specific, system-wide analysis. This can flag risks and pinpoint specific actions to protect medicine quality, and thus health.
机译:简介:不合标准和伪造的药物破坏卫生系统。我们试图解开推动这些产品的生产的政治和经济因素,并解释他们如何到达患者。方法:我们在中国,印度尼西亚,土耳其和罗马尼亚进行了深入的案例研究。我们审查了学术论文,并按报告(n = 840),开发半结构化问卷。我们采访了监管机构,政策制定者,制药制造商,医生,药剂师,患者和学者(n = 88)。我们使用NVivo软件编码数据,并开发了分析框架,以评估不合标准和伪造的药物的国家风险。我们测试了对世界卫生组织报告的案件的框架,从所有收入水平的国家。结果:我们发现,对提供普遍健康保险的政治承诺导致了旨在降低医疗产品价格的公共采购政策。在响应,合法的利润驱动的制药公司通过减少成本来保护他们的利润,或退出较少的有利可图的市场,而分销商从事套利。与此同时,卫生服务提供者有时通过“upselling”患者保护利润保护未被保险公司未涵盖的药物。成本切割可能会破坏质量保证,导致药物不合标准或降解。其他响应有助于短缺,不合理的需求和高价格。所有这些都为伪造产品生产者提供市场机会;他们还推动了常规供应链之外的消费者,提供伪造者,方便地访问客户。分析框架在大多数高收入设置中捕获这些互动的情况;最贫穷国家运营的其他因素。结论:大多数努力确保医学质量目前专注于产品监管。然而,我们的研究表明市场机制是质量差的主要司机,包括普遍保健覆盖的政治承诺。我们制定了一个框架,以指导特定国家,全系统的分析。这可以标志着风险并确定特定的动作来保护药物质量,从而保持健康。

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