The National Bioethics Advisory Commission

Contributing to Public Policy

by Elisa Eiseman

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The National Bioethics Advisory Commission (NBAC) was established by executive order in 1995 to advise the National Science and Technology Council and other government entities on bioethical issues arising from research on human biology and human behavior. During the commission’s five-year tenure, it submitted six major reports to the White House that contained 120 recommendations on several complex bioethical issues, including the cloning of human beings, research involving persons with mental disorders that may affect decisionmaking capacity, research with human biological materials, embryonic stem cell research, U.S.-sponsored clinical trials in developing countries, and protection of human research participants. This RAND study was conducted to assess NBAC’s contribution to the policymaking process as it relates to these issues. The author provides a detailed account of the responses to each of NBAC’s six reports from the president, Congress, government, societies and foundations, other countries, and international organizations. Although no legislation has been passed based on NBAC’s recommendations, agencies responsible for a major portion of federally funded research involving human participants-particularly the National Institutes of Health-have adopted several of NBAC’s recommendations and issued research guidelines based on those recommendations.

Table of Contents

  • Chapter One

    Introduction

  • Chapter Two

    NBAC in the Public Eye

  • Chapter Three

    Response to the Cloning Human Beings Report

  • Chapter Four

    Response to the Research Involving Persons with Mental Disorders That May Affect Decisionmaking Capacity Report

  • Chapter Five

    Response to the Research Involving Human Biological Materials: Ethical Issues and Policy Guidance Report

  • Chapter Six

    Response to the Ethical Issues in Human Stem Cell Research Report

  • Chapter Seven

    Response to the Ethical and Policy Issues in International Research: Clinical Trials in Developing Countries Report

  • Chapter Eight

    Response to the Ethical and Policy Issues in Research Involving Human Participants Report

  • Chapter Nine

    Summary

  • Appendix

    Data Collection Methods

The research described in this report was conducted by RAND's Science and Technology Policy Institute for the National Bioethics Advisory Commission.

This report is part of the RAND Corporation Monograph report series. The monograph/report was a product of the RAND Corporation from 1993 to 2003. RAND monograph/reports presented major research findings that addressed the challenges facing the public and private sectors. They included executive summaries, technical documentation, and synthesis pieces.

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