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Cost benefit of investment on quality in pharmaceutical manufacturing: WHO GMP pre- and post-certification of a Nigerian pharmaceutical manufacturer

机译:药品生产质量投资的成本效益:尼日利亚药品生产商的WHO GMP认证前后

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Background Pharmaceutical companies in Africa need to invest in both facilities and quality management systems to achieve good manufacturing practice (GMP) compliance. Compliance to international GMP standards is important to the attainment of World Health Organization (WHO) prequalification. However, most of the local pharmaceutical manufacturing companies may be deterred from investing in quality because of many reasons, ranging from financial constraints to technical capacity. This paper primarily evaluates benefits against the cost of investing in GMP, using a Nigerian pharmaceutical company, Chi Pharmaceuticals Limited, as a case study. This paper also discusses how to drive more local manufacturers to invest in quality to attain GMP compliance; and proffers practical recommendations for local manufacturers who would want to invest in quality to meet ethical and regulatory obligations. Method The cost benefit of improving the quality of Chi Pharmaceuticals Limited’s facilities and system to attain WHO GMP certification for the production of zinc sulfate 20-mg dispersible tablets was calculated by dividing the annual benefits derived from quality improvement interventions by the annual costs of implementing quality improvement interventions, referred to as a benefit-cost ratio (BCR). Result Cost benefit of obtaining WHO GMP certification for the production of zinc sulfate 20-mg dispersible tablets was 5.3 (95% confidence interval of 5.0–5.5). Conclusion Investment in quality improvement intervention is cost-beneficial for local manufacturing companies. Governments and regulators in African countries should support pharmaceutical companies striving to invest in quality. Collaboration of local manufacturing companies with global companies will further improve quality. Local pharmaceutical companies should be encouraged to key into development opportunities available for pharmaceutical companies in Africa.
机译:背景技术非洲的制药公司需要在设施和质量管理系统上进行投资,以实现良好生产规范(GMP)。符合国际GMP标准对于获得世界卫生组织(WHO)资格预审至关重要。但是,由于多种原因,从财务限制到技术能力,大多数本地制药公司可能会阻止对质量的投资。本文主要以尼日利亚制药公司Chi Pharmaceuticals Limited作为案例研究,对照投资GMP的成本评估收益。本文还讨论了如何推动更多的本地制造商对质量进行投资,以达到GMP要求。并为希望在质量上进行投资以符合道德和监管义务的本地制造商提供实用建议。方法通过将质量改进措施产生的年度收益除以实施质量的年度成本,计算出改善Chi Pharmaceuticals Limited的设施和系统质量以获得WHO WHO GMP认证的20毫克硫酸锌分散片生产的成本收益。改善干预措施,称为效益成本比(BCR)。结果获得用于生产20毫克硫酸锌分散片的WHO GMP认证的成本效益为5.3(95%置信区间为5.0-5.5)。结论对质量改进干预措施的投资对本地制造公司而言是成本有利的。非洲国家的政府和监管机构应支持努力投资质量的制药公司。本地制造公司与跨国公司的合作将进一步提高质量。应鼓励当地制药公司抓住非洲制药公司可利用的发展机会。

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