Workshop on risk assessment in reproductive and developmental toxicology: addressing the assumptions and identifying the research needs

Regul Toxicol Pharmacol. 1989 Oct;10(2):110-22. doi: 10.1016/0273-2300(89)90018-4.

Abstract

The risk assessment process is an imprecise procedure aimed at determining a toxicant exposure level with an acceptable risk to the human population. The lack of precision is due to the uncertainties in the assumptions that must be made due to the lack of specific scientific information or knowledge of how to use certain types of data. Unfortunately, every necessary piece of information cannot be obtained for every chemical requiring a risk assessment. In order to better identify and understand some of the assumptions that are made in the risk assessment of reproductive and developmental toxicants, a workshop was organized to specifically define the assumptions underlying the risk assessments for seven specific toxicants (dibromochloropropane, dioxin, glycol ethers, heptachlor, lead, tetrahydrocannabinol, and vitamin A) and to determine the potential research which would reduce the uncertainty associated with making those assumptions. The major assumptions discussed centered around the topics of heterogeneous populations, thresholds, safety factors, exposure assessment, quantitative structure-activity relationships, and mechanisms. This report is the summary of the workshop discussions.

Publication types

  • Review

MeSH terms

  • Animals
  • Humans
  • Reproduction / drug effects*
  • Research
  • Risk
  • Structure-Activity Relationship
  • Teratogens*

Substances

  • Teratogens