1990
DOI: 10.1177/026119299001800131.1
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Report and Recommendations of the CAAT/ERGATT Workshop on the Validation of Toxicity Test Procedures

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Cited by 100 publications
(51 citation statements)
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“…Already in 1990, an international committee under participation of ZEBET convened to develop a scientific concept for the experimental validation of toxicological testing methods (Balls et al 1990 ). Followed by two similar workshops (Balls et al 1995 ), and two OECD workshops in 1996 and 2002 (Organisation for Economic Co-Operation, Development 1996 , 2002 ), this ultimately led to the OECD Guidance Document No.…”
Section: Current Efforts At Zebetmentioning
confidence: 99%
“…Already in 1990, an international committee under participation of ZEBET convened to develop a scientific concept for the experimental validation of toxicological testing methods (Balls et al 1990 ). Followed by two similar workshops (Balls et al 1995 ), and two OECD workshops in 1996 and 2002 (Organisation for Economic Co-Operation, Development 1996 , 2002 ), this ultimately led to the OECD Guidance Document No.…”
Section: Current Efforts At Zebetmentioning
confidence: 99%
“…The future of alternatives research lies in validation. The validation of alternative tests is the process by which the reliability and relevance of a test are established for a particular purpose (Balls et al, ). Over the last 12 years, the European Centre for the Validation of Alternative Methods (ECVAM), in cooperation with international experts, has set up guidelines for validation, and five stages in the evolution of a new test were defined: development, prevalidation, validation, peer review , and regulatory acceptance .…”
Section: The Concept Of Validationmentioning
confidence: 99%
“…Against a background of good progress in developing some in vitro tests to predict acute eye and skin toxicity (8,9), efforts were focused on defining processes for the validation of new tests -recognising that transparent and rigorous evaluations of the relevance and reliability of these new methods would be essential for their wider scientific and regulatory acceptance and implementation. We started off in a cooperative manner, with the initial workshops on validation principles and processes involving both European and American scientists and regulators (10,11). During this period, the first inhouse company safety testing strategies for minimising or avoiding animal studies for local (eye and skin) effects were also being presented and published (for example, 12).…”
Section: Stage 1: 1990-1994mentioning
confidence: 99%