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OLS Field Name OLS Field Data
Main Title What Can Be Learnt from Protocols Relating to Non-Pharmaceuticals.
Author Kimmel, C. A. ;
CORP Author Environmental Protection Agency, Washington, DC. Office of Health and Environmental Assessment.
Publisher May 91
Year Published 1991
Report Number EPA/600/A-92/020 ;OHEA-R-437;
Stock Number PB92-150424
Additional Subjects Pesticides ; Toxicity ; Guidelines ; Teratogens ; Nervous system ; Test methods ; Reproduction(Biology) ; Fertility ; Risk assessment ; Humans ; Health hazards ; Reprints ; Toxicity testing protocols ; Toxic Substances Control Act ; Federal Insecticide Fungicide and Rodenticide Act
Holdings
Library Call Number Additional Info Location Last
Modified
Checkout
Status
NTIS  PB92-150424 Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy. 08/28/1992
Collation 20p
Abstract 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.
Supplementary Notes 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 Symposium paper.
Title Annotations Reprint: What Can Be Learnt from Protocols Relating to Non-Pharmaceuticals.
Category Codes 68E; 57Y
NTIS Prices PC A03/MF A01
Primary Description 600/21
Document Type NT
Cataloging Source NTIS/MT
Control Number 211522609
Origin NTIS
Type CAT