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REFERENCE DOSE (RFD): DESCRIPTION AND USE IN HEALTH RISK ASSESSMENTS

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Archived files are provided for reference purposes only. The file was current when produced, but is no longer maintained and may now be outdated. Persons with disabilities having difficulty accessing archived files may contact the Risk Webmaster for assistance. Please use the contact us form if you need additional support.

Abstract

For many years the concept of the "acceptable daily intake" has served the toxicological and regulatory fields quite well. owever, as approaches to assessing the health significance of exposures to noncarcinogenic substances receive greater scrutiny, some difficulties with this traditional approach have become more apparent. Consequently, the concept of the "reference dose" is introduced in order to avoid use of prejudicial terms (e.g. , "safety" and "acceptable"), to promote greater consistency in the assessment of noncarcinogenic chemicals, and to maintain the functional separation between risk assessment and risk management

Citation

Barnes, D. AND M. Dourson. REFERENCE DOSE (RFD): DESCRIPTION AND USE IN HEALTH RISK ASSESSMENTS. U.S. Environmental Protection Agency, Washington, D.C., EPA/600/J-88/310 (NTIS PB89202436), 1989.

History/Chronology

Additional Information

Regulatory Toxicology and Pharmacology, 8:471-486, 1988

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  • REFERENCE DOSE (RFD): DESCRIPTION AND USE IN HEALTH RISK ASSESSMENTS
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Last updated on January 03, 2006
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