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扩大基本药物的全球可及性:可持续加强医疗产品监管体系的投资重点。

Expanding global access to essential medicines: investment priorities for sustainably strengthening medical product regulatory systems.

机构信息

United States Pharmacopeia, Rockville, USA.

Global Medicines Program, School of Pharmacy, School of Public Health, University of Washington, Seattle, USA.

出版信息

Global Health. 2018 Nov 1;14(1):102. doi: 10.1186/s12992-018-0421-2.

Abstract

Access to quality-assured medical products improves health and save lives. However, one third of the world's population lacks timely access to quality-assured medicines while estimates indicate that at least 10% of medicine in low- and middle-income countries (LMICs) are substandard or falsified (SF), costing approximately US$ 31 billion annually. National regulatory authorities are the key government institutions that promote access to quality-assured medicines and combat SF medical products but despite progress, regulatory capacity in LMICs is still insufficient. Continued and increased investment in regulatory system strengthening (RSS) is needed. We have therefore reviewed existing global normative documents and resources and engaged with our networks of global partners and stakeholders to identify three critical challenges being faced by NRAs in LMICs that are limiting access to medical products and impeding detection of and response to SF medicines. The challenges are; implementing value-added regulatory practices that best utilize available resources, a lack of timely access to new, quality medical products, and limited evidence-based data to support post-marketing regulatory actions. To address these challenges, we have identified seven focused strategies; advancing and leveraging convergence and reliance initiatives, institutionalizing sustainability, utilizing risk-based approaches for resource allocation, strengthening registration efficiency and timeliness, strengthening inspection capacity and effectiveness, developing and implementing risk-based post-marketing quality surveillance systems, and strengthening regulatory management of manufacturing variations. These proposed solutions are underpinned by 13 focused recommendations, which we believe, if financed, technically supported and implemented, will lead to stronger health system and as a consequence, positive health outcomes.

摘要

获得有质量保证的医疗产品可以改善健康状况并挽救生命。然而,世界上有三分之一的人口无法及时获得有质量保证的药品,而据估计,至少 10%的中低收入国家的药品是劣药或假药(SF),每年造成的损失约为 310 亿美元。国家监管机构是促进获得有质量保证的药品和打击 SF 医疗产品的关键政府机构,但尽管取得了进展,中低收入国家的监管能力仍然不足。需要继续和增加对监管系统强化(RSS)的投资。因此,我们审查了现有的全球规范文件和资源,并与我们的全球合作伙伴和利益攸关方网络进行了接触,以确定国家监管机构在中低收入国家面临的三个限制获得医疗产品和阻碍发现和应对 SF 药品的关键挑战。这些挑战是:实施增值监管做法,以最佳利用现有资源;缺乏及时获得新的高质量医疗产品的渠道;以及支持上市后监管行动的基于证据的有限数据。为了应对这些挑战,我们确定了七个重点战略:推进和利用趋同和依赖倡议、使可持续性制度化、利用基于风险的方法进行资源分配、加强注册效率和及时性、加强检查能力和效果、开发和实施基于风险的上市后质量监测系统,以及加强对制造变更的监管管理。这些拟议的解决方案以 13 项重点建议为基础,如果得到资金支持、技术支持和实施,我们相信这些解决方案将导致更强大的卫生系统,并因此带来积极的健康结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac07/6211488/257b54a3c353/12992_2018_421_Fig1_HTML.jpg

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