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Books and Articles

• Appelbaum. Paul S.. and Rosenbaurn. Alan. “Tarasoff and the Researcher: Does the Duty to Protect Apply in the Research Setting?” American Psychologist 44 (No.6. June 1989): 885-894.
• Beaucharnp, Tom L.: Faden. Ruth R.: Wallace. R. Jay, Jr.: and Waiters. LeRoy. eds. Ethical Issues in Social Science Research. Baltimore, MD: Johns Hopkins University Press. 1982.
• Beecher, Henry K. Research and the Individual: Human Studies. Boston: Little, Brown and Company, 1970.
• Benson. P.R. “The Social Control of Human Biomedical Research: An Overview and Review of the Literature.” Social Science and Medicine 29 (No.1, .1989): 1-12.
• Bernard, Claude. An Introduction to the Study of Experimental Medicine, translated by N.C. Greene. New York: The Macmillan Company, 1927.
• Greenwald, Robert A,; Ryan, Mary Kay: and Mulvihill, James E.. eds. Human Subjects Research: A Handbook for Institutional Review Boards. New York and London: Plenum Press. 1982.
• Sieber, Joan E. “Planning Ethically Responsible Research: A Guide for Students and Internal Review Boards.” Applied Social Research Methods Series, vol. 31. Newbury Park. CA: Sage Publications, 1992.

Journals

Computer Search Services

Recordings

• Columbia University Seminars on Media and Society, in association with WNET New York.
• Human Experiment. Produced by Betsy Miller and Martha Elliott. Annenberg: CPB Project. 1989.
• National Library of Medicine. Evolving Concern: Protection of Human Subjects. Produced for the U.S. National Institutes of Health and the U.S. Food and Drug Administration. Bethesda. MD: National Institutes of Health, Office for Protection from Research Risks, 1986.
• National Library of Medicine. The Belmont Report: Basic Ethical Principles and the Application. Produced and written for the U.S. National Institutes of Health and the U.S. Food and Drug Administration by Michael D. Hamilton. Bethesda, MD: National Institutes of Health, Office for Protection from Research Risks, 1986.
• National Library of Medicine. Balancing Society’s Mandates: IRB Review Criteria. Produced for the U.S. National Institutes of Health and the U.S. Food and Drug Administration. Bethesda. MD: National Institutes of Health, Office for Protection from Research Risks, 1986.

Web pages and ListServs

• OHRP-L@LIST.NIH.GOV Essential!! All major OUR Updates. To subscribe, see the OHRP-L web page.
• University of Minnesota, IRB Home Page. Many useful parts.

Other IRB documents

• Request for IRB Clearance (PDF)
• Criteria for Informed Consent and Assent
• Criteria for Exempt Status
• Criteria for Expedited Review
• Request for Full IRB Review (PDF)
• Request for Continuing Review (PDF)
• IRB Home

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