The validation and acceptance of alternatives to animal testing

被引:29
作者
Balls, M [1 ]
Fentem, JH [1 ]
机构
[1] Commiss European Communities, Joint Res Ctr, Inst Hlth & Consumer Protect, ECVAM, I-21020 Ispra, VA, Italy
关键词
animal testing; in vitro toxicology; prediction model; replacement alternatives; regulatory testing; toxicity testing; validation;
D O I
10.1016/S0887-2333(99)00067-3
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Validation is the key to the regulatory status of alternative methods. A series of questions are put. to which answers are given, including the following: What is validation? What is meant by "relevance", "reliability" and "purpose"? Why and when is formal validation necessary? What comes before and after a formal validation study? How have validation criteria been defined, and to what extent have they been harmonized internationally? How are validation studies set up, managed and funded? What is a test? Do prediction models have to be validated? What is prevalidation? What is acceptance, and who is responsible for acceptance? How are validation studies reported? How should a validated test be defined and recognized? Must all new tests be validated? Are the same standards being applied to new in vitro and new in vivo tests? Has validation been successful so far? What can be done to improve validation? Is validation helping or hindering the development of in vine toxicology and the implementation of the 'Three Rs' of Russell & Burch? (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:837 / 846
页数:10
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