||What Can Be Learnt from Protocols Relating to Non-Pharmaceuticals.
Kimmel, C. A. ;
||Environmental Protection Agency, Washington, DC. Office of Health and Environmental Assessment.
Nervous system ;
Test methods ;
Risk assessment ;
Health hazards ;
Toxicity testing protocols ;
Toxic Substances Control Act ;
Federal Insecticide Fungicide and Rodenticide Act
||Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy.
||Under the Toxic Substances Control Act (TSCA), reproductive and developmental toxicity studies are required on a case-by-case basis depending on whether or not there is reason to suspect that an agent may have reproductive or developmental effects, or if production and/or release of a chemical is likely to be substantial. Under the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA), standard developmental toxicity studies in two species and a two-generation reproduction study in rats are required for all food use pesticides and for non-food use pesticides when exposure is likely. Developmental neurotoxicity studies are required in cases where indications from other data suggest concern. The EPA has also developed guidelines for reproductive and developmental toxicity risk assessment that describe the evaluation of data for extrapolation to humans. These guidelines provide the basic assumptions that are made in the risk assessment process and the procedures used to estimate exposure levels that are not expected to increase the risk for reproductive or developmental effects above background incidence rates. Data from developmental toxicity, developmental neurotoxicity and reproduction studies form the primary data base used in reproductive and developmental toxicity risk assessments, but may be enhanced by data from other studies, including pharmacokinetic and mechanistic studies. The development of risk assessment guidance has been extremely helpful in identifying data needed for reducing uncertainties, eliminating assumptions and improving the qualitative and quantitative extrapolation of data to exposed human populations.
||See also PB86-108958, PB90-161530 and PB91-154617. Presented at a workshop on Current Issues in Reproductive and Developmental Toxicology, London, U.K. in May 1991.
|NTIS Title Notes
||Reprint: What Can Be Learnt from Protocols Relating to Non-Pharmaceuticals.
||PC A03/MF A01