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钩端螺旋体疫苗效力测试的国际监管要求。圆桌会议:当前要求及协调机会。

International regulatory requirements for Leptospira vaccine potency testing. Roundtable: current requirements and opportunity for harmonization.

作者信息

Draayer Hans A, Bruckner Lukas, Peña-Moctezuma Alejandro de la, Srinivas Geetha

机构信息

Gourdneck View Consulting, LLC, Portage, MI 49002, USA.

出版信息

Biologicals. 2013 Sep;41(5):305-7. doi: 10.1016/j.biologicals.2013.06.008. Epub 2013 Jul 23.

Abstract

Progress continues to be made in the ongoing efforts to replace, reduce, or refine the use of laboratory animals for Leptospira vaccine potency testing in certain markets/regions. Leptospira-containing vaccines, as with many veterinary vaccines, are manufactured and distributed both on a regional basis by local manufacturers and internationally by large multinational firms. Three general scenarios exist for the international testing and distribution of veterinary vaccines including: 1) the importing country recognizes the country of origin's testing and batch release data with no additional testing; 2) the importing country requires the manufacturer to conduct a specific potency assay based on the current importing market's regulations for the importing country or 3) the importing country requires retesting of the product in country prior to distribution. Scenarios 2 and 3 both have the potential to significantly increase the usage of laboratory animals for what may be considered redundant testing. Specific requirements for the importation of Leptospira vaccines in the United States, Europe, and Mexico were presented as well as efforts to reduce the use of laboratory animal testing through the availability of internationally recognized tests.

摘要

在某些市场/地区,为钩端螺旋体疫苗效力测试而进行的替代、减少或优化实验动物使用的持续努力仍在取得进展。与许多兽用疫苗一样,含钩端螺旋体的疫苗由当地制造商在区域范围内生产和分销,也由大型跨国公司在国际上生产和分销。兽用疫苗的国际测试和分销存在三种一般情况,包括:1)进口国认可原产国的测试和批次放行数据,无需额外测试;2)进口国要求制造商根据当前进口市场对进口国的规定进行特定的效力测定;或3)进口国要求在产品分销前在国内重新进行测试。情况2和情况3都有可能显著增加用于可能被视为冗余测试的实验动物的使用量。介绍了美国、欧洲和墨西哥对钩端螺旋体疫苗进口的具体要求,以及通过提供国际认可的测试来减少实验动物测试使用的努力。

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