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医疗产品监管协调:提高东非共同体监管能力的关键因素。

Harmonization of medical products regulation: a key factor for improving regulatory capacity in the East African Community.

作者信息

Ndomondo-Sigonda Margareth, Miot Jacqueline, Naidoo Shan, Masota Nelson E, Ng'andu Brian, Ngum Nancy, Kaale Eliangiringa

机构信息

Pharmacology Division, Department of Pharmacy and Pharmacology, Faculty of Health Sciences, University of Witwatersrand, Johannesburg, South Africa.

African Union Development Agency -New Partnership for Africa's Development (AUDA-NEPAD), Midrand, South Africa.

出版信息

BMC Public Health. 2021 Jan 21;21(1):187. doi: 10.1186/s12889-021-10169-1.

Abstract

BACKGROUND

Limited capacity to regulate medical products is associated with circulation of products which do not meet standards of quality, safety and efficacy with negative public health and economic outcomes. This study focused on assessing the effect of the East African Community (EAC) medicines regulatory harmonization initiative on the capacity of national medicines regulatory agencies, with a focus on registration and inspection systems.

METHODS

An exploratory mixed-method design using both qualitative and quantitative data to access data from six national medicines regulatory authorities (NMRAs) and the EAC Secretariat. Data was collected using a combination of semi-structured interviews, questionnaires, and checklists for the period 2010/11-2015/16 with 2010/11 data serving as baseline. Heads of NMRAs, regulatory and monitoring and evaluation experts, and the EAC Secretariat Project Officer were enrolled in the study. A set of 14 indicators grouped into 6 categories were used to assess NMRAs performance.

RESULTS

Policy and legal frameworks provide a foundation for effective regulation. Collaboration, harmonization, joint dossier reviews and inspections of manufacturing sites, reliance and cooperation are key factors for building trust and capacity among NMRAs. Five out of six of the EAC Partner States have comprehensive medicines laws with autonomous NMRAs. All the NMRAs have functional registration and good manufacturing practice inspection systems supported by regional harmonised guidelines for registration, inspection, quality management and information management systems with four NMRAs attaining ISO 9001:2015 certification.

CONCLUSIONS

The EAC regulatory harmonization initiative has contributed to improved capacity to regulate medical products. The indicators generated from this research can be replicated for evaluation of similar initiatives across and beyond the African continent and contribute to public health policy.

摘要

背景

医疗产品监管能力有限与不符合质量、安全和疗效标准的产品流通相关,会对公众健康和经济产生负面影响。本研究聚焦于评估东非共同体(EAC)药品监管协调倡议对国家药品监管机构能力的影响,重点关注注册和检查系统。

方法

采用探索性混合方法设计,使用定性和定量数据从六个国家药品监管当局(NMRA)和东非共同体秘书处获取数据。在2010/11 - 2015/16期间,通过半结构化访谈、问卷和清单相结合的方式收集数据,以2010/11年的数据作为基线。参与研究的人员包括国家药品监管当局负责人、监管及监测与评估专家以及东非共同体秘书处项目官员。使用一组分为6类的14项指标来评估国家药品监管当局的绩效。

结果

政策和法律框架为有效监管提供了基础。合作、协调、联合档案审查和生产场地检查、信任和合作是在国家药品监管当局之间建立信任和能力的关键因素。东非共同体六个伙伴国家中有五个拥有全面的药品法律以及自主的国家药品监管当局。所有国家药品监管当局都具备有效的注册和良好生产规范检查系统,并得到区域统一的注册、检查、质量管理和信息管理系统指南的支持,其中四个国家药品监管当局获得了ISO 9001:2015认证。

结论

东非共同体监管协调倡议有助于提高医疗产品监管能力。本研究得出的指标可用于在非洲大陆内外评估类似倡议,并为公共卫生政策提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9d7/7818747/83f624b1bfc7/12889_2021_10169_Fig1_HTML.jpg

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