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疫苗授权的监管要求。

Regulatory requirements for vaccine authorisation.

作者信息

Jones P G H, Cowan G, Gravendyck M, Nagata T, Robinson S, Waits M

机构信息

International Federation for Animal Health, rue Defacqz, 1, 1000 Brussels, Belgium.

出版信息

Rev Sci Tech. 2007 Aug;26(2):379-93.

Abstract

Vaccines are one of the most important tools available in the prevention and control of diseases in animals. It is therefore of the utmost importance that when vaccines are used, such use should meet with the requirements of the World Organisation for Animal Health Terrestrial Animal Health Code and must be authorised by the recognised licensing body in the country/region where the vaccines are to be used, in accordance with the three key criteria of quality, safety and efficacy. This article provides a comprehensive and comparative description of the regulatory requirements in place for veterinary vaccines in major regions of the world, highlighting the similarities and pointing out also where there are differences. Recent advances in harmonisation of such testing requirements achieved through the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH) are also described. The contents will provide a valuable guide to those engaged in the research and development of vaccines globally, and reassure those involved in the prevention and control of animal diseases that veterinary vaccines, when fully authorised and used according to the label instructions, are safe and efficacious.

摘要

疫苗是预防和控制动物疾病的最重要工具之一。因此,极其重要的是,在使用疫苗时,这种使用应符合世界动物卫生组织《陆生动物卫生法典》的要求,并且必须根据质量、安全性和有效性这三个关键标准,得到疫苗使用所在国家/地区认可的许可机构的授权。本文全面且比较性地描述了世界主要地区对兽用疫苗的监管要求,突出了相似之处,并指出了差异所在。还介绍了通过兽药注册技术要求国际协调合作组织(VICH)在统一此类检测要求方面取得的最新进展。这些内容将为全球从事疫苗研发的人员提供宝贵指导,并让参与动物疾病预防和控制的人员放心,即兽用疫苗在获得充分授权并按照标签说明使用时是安全有效的。

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