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The role of in vitro toxicology with respect to regulatory testing is discussed with particular reference to: EU legislation and the role of the European Centre for the Validation of Alternative Methods (ECVAM); problems with the validation process; regulatory acceptance criteria; and the ECVAM prevalidation scheme.

Additional information

Authors: BALLS M, JRC Ispra (IT)
Bibliographic Reference: Paper presented: GRETOX '95: 33rd International Congress on Forensic Toxicology/1st International Congress on Environmental Toxicology, Thessaloniki (GB), August 27-31, 1995
Availability: Available from (1) as Paper EN 39633 ORA
Record Number: 199610611 / Last updated on: 1996-05-27
Original language: en
Available languages: en