• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

将3R方法纳入世界卫生组织生物制品批放行检测指南:NC3R提交给世界卫生组织生物标准化专家委员会的最终报告摘要

Integrating 3Rs approaches in WHO guidelines for the batch release testing of biologicals: Summary of NC3Rs final report to WHO Expert Committee for Biological Standardisation.

作者信息

Lilley Elliot, Isbrucker Richard, Holmes Anthony

机构信息

NC3Rs, London, United Kingdom.

Health Canada, Ottawa, Canada.

出版信息

Biologicals. 2025 Feb;89:101778. doi: 10.1016/j.biologicals.2024.101778. Epub 2024 Dec 20.

DOI:10.1016/j.biologicals.2024.101778
PMID:39708625
Abstract

A recently published report from the UK National Centre for the Replacement, Refinement, and Reduction of Animals in Research (NC3Rs) has highlighted significant opportunities for the broader inclusion of 3Rs approaches (i.e. Replacement, Reduction and Refinement of animal tests) within World Health Organization (WHO) manuals, guidelines and recommendations for vaccines and biotherapeutics. The report is the culmination of a three-year project, co-funded by the Bill & Melinda Gates Foundation, to review the extent to which animal-based testing methods are described in WHO manuals, guidelines and recommendations. The aim was to identify where recommendations did not incorporate current non-animal testing strategies and/or 3Rs principles in biologicals quality control and batch release testing. The inclusion of such methods in WHO guidance documents would improve their adoption by regulators and help to accelerate the safe release of these products to the communities who need them most. The final report was presented to the WHO's Expert Committee on Biological Standardization (ECBS) in October 2023 for their consideration and response. The project findings and recommendations described in the report are summarised in this article.

摘要

英国国家动物研究替代、优化与减少中心(NC3Rs)最近发布的一份报告强调,在世界卫生组织(WHO)关于疫苗和生物治疗药物的手册、指南及建议中,更广泛地纳入3R方法(即替代、减少和优化动物试验)存在重大机遇。该报告是一个为期三年项目的成果,该项目由比尔及梅琳达·盖茨基金会共同资助,旨在审查WHO手册、指南和建议中对基于动物的检测方法的描述程度。目的是确定在生物制品质量控制和批次放行检测中,哪些建议未纳入当前的非动物检测策略和/或3R原则。将此类方法纳入WHO指导文件将提高监管机构对它们的采用率,并有助于加速这些产品向最需要它们的社区安全放行。最终报告于2023年10月提交给WHO生物标准化专家委员会(ECBS)以供其审议和回应。本文总结了报告中描述的项目发现和建议。

相似文献

1
Integrating 3Rs approaches in WHO guidelines for the batch release testing of biologicals: Summary of NC3Rs final report to WHO Expert Committee for Biological Standardisation.将3R方法纳入世界卫生组织生物制品批放行检测指南:NC3R提交给世界卫生组织生物标准化专家委员会的最终报告摘要
Biologicals. 2025 Feb;89:101778. doi: 10.1016/j.biologicals.2024.101778. Epub 2024 Dec 20.
2
Integrating 3Rs approaches in WHO guidelines for the batch release testing of biologicals: Reports from a series of NC3Rs stakeholder workshops.将3R方法纳入世界卫生组织生物制品批签发检测指南:一系列NC3R利益相关方研讨会的报告
Biologicals. 2025 Feb;89:101777. doi: 10.1016/j.biologicals.2024.101777. Epub 2024 Dec 20.
3
Integrating 3Rs approaches in WHO guidelines for the batch release testing of biologicals.将 3Rs 方法纳入世卫组织生物制品分批放行检测指南。
Biologicals. 2021 Nov;74:24-27. doi: 10.1016/j.biologicals.2021.10.002. Epub 2021 Nov 6.
4
Integrating 3Rs approaches in WHO guidelines for the batch release testing of biologicals: Responses from a survey of vaccines and biological therapeutics manufacturers.将 3Rs 方法整合到世卫组织生物制品批量放行检测指南中:来自疫苗和生物治疗药物制造商调查的回应。
Biologicals. 2023 Feb;81:101660. doi: 10.1016/j.biologicals.2022.11.002. Epub 2022 Nov 12.
5
Integrating 3Rs approaches in WHO guidelines for the batch release testing of biologicals: Responses from a survey of National Control Laboratories and National Regulatory Authorities.将 3Rs 方法整合到世卫组织生物制品分批放行检测指南中:来自国家控制实验室和国家监管机构调查的回应。
Biologicals. 2023 Nov;84:101721. doi: 10.1016/j.biologicals.2023.101721. Epub 2023 Nov 1.
6
Evaluation of cell substrates for the production of biologicals: Revision of WHO recommendations. Report of the WHO Study Group on Cell Substrates for the Production of Biologicals, 22-23 April 2009, Bethesda, USA.生物制品生产用细胞基质的评估:世界卫生组织建议的修订。世界卫生组织生物制品生产用细胞基质研究小组报告,2009年4月22 - 23日,美国贝塞斯达
Biologicals. 2010 Jan;38(1):162-9. doi: 10.1016/j.biologicals.2009.08.019. Epub 2009 Oct 8.
7
3Rs implementation in veterinary vaccine batch-release testing: Current state-of-the-art and future opportunities. A webinar and workshop report.3Rs 在兽医疫苗批次放行检测中的实施:现状与未来机遇。网络研讨会和研讨会报告。
Biologicals. 2023 Aug;83:101695. doi: 10.1016/j.biologicals.2023.101695. Epub 2023 Jul 27.
8
WHO Expert Committee on Biological Standardization.世界卫生组织生物标准化专家委员会
World Health Organ Tech Rep Ser. 2016(999):1-267.
9
Who Expert Committee on Biological Standardization.生物标准化专家委员会。
World Health Organ Tech Rep Ser. 2004;926:1-109.
10
WHO Expert Committee on Biological Standardization. Sixty-fifth report.世界卫生组织生物标准化专家委员会。第六十五次报告。
World Health Organ Tech Rep Ser. 2015(993):1-262.