62 found
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  1.  76
    Ethics and Regulation of Clinical Research.Robert J. Levine - 1986 - Urban & Schwarzenberg.
    In this book, Dr. Robert J. Levine reviews federal regulations, ethical analysis, and case studies in an attempt to answer these questions.
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  2. Informed Consent: Some Challenges to the Universal Validity of the Western Model.Robert J. Levine - 1991 - Journal of Law, Medicine and Ethics 19 (3-4):207-213.
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  3.  13
    Informed Consent: Some Challenges to the Universal Validity of the Western Model.Robert J. Levine - 1991 - Journal of Law, Medicine and Ethics 19 (3-4):207-213.
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  4.  10
    Building a New Consensus: Ethical Principles and Policies for Clinical Research on HIV / AIDS.Carol Levine, Nancy Neveloff Dubler & Robert J. Levine - 1991 - IRB: Ethics & Human Research 13 (1/2):194-210.
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  5.  13
    Clarifying the Concepts of Research Ethics.Robert J. Levine - 1979 - Hastings Center Report 9 (3):21-26.
  6.  47
    Social Contexts Influence Ethical Considerations of Research.Robert J. Levine, Carolyn M. Mazure, Philip E. Rubin, Barry R. Schaller, John L. Young & Judith B. Gordon - 2011 - American Journal of Bioethics 11 (5):24-30.
    This article argues that we could improve the design of research protocols by developing an awareness of and a responsiveness to the social contexts of all the actors in the research enterprise, including subjects, investigators, sponsors, and members of the community in which the research will be conducted. ?Social context? refers to the settings in which the actors are situated, including, but not limited to, their social, economic, political, cultural, and technological features. The utility of thinking about social contexts is (...)
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  7.  27
    Pharmaceutical Research Involving the Homeless.Tom L. Beauchamp, Bruce Jennings, Eleanor D. Kinney & Robert J. Levine - 2002 - Journal of Medicine and Philosophy 27 (5):547 – 564.
    Discussions of research involving vulnerable populations have left the homeless comparatively ignored. Participation by these subjects in drug studies has the potential to be upsetting, inconvenient, or unpleasant. Participation occasionally produces injury, health emergencies, and chronic health problems. Nonetheless, no ethical justification exists for the categorical exclusion of homeless persons from research. The appropriate framework for informed consent for these subjects of pharmaceutical research is not a single event of oral or written consent, but a multi-staged arrangement of disclosure, dialogue, (...)
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  8.  17
    The Impact of HIV Infection on Society's Perception of Clinical Trials.Robert J. Levine - 1994 - Kennedy Institute of Ethics Journal 4 (2):93-98.
  9.  1
    Editorial: The "Best Proven Therapeutic Method" Standard in Clinical Trials in Technologically Developing Countries.Robert J. Levine - 1998 - IRB: Ethics & Human Research 20 (1):5.
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  10.  9
    The Use of Placebos in Randomized Clinical Trials.Robert J. Levine - 1985 - IRB: Ethics & Human Research 7 (2):1.
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  11.  9
    The Nature, Scope, and Justification of Clinical Research.Robert J. Levine - 2008 - In Ezekiel J. Emanuel (ed.), The Oxford Textbook of Clinical Research Ethics. Oxford University Press. pp. 211.
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  12. Research Ethics Committees.Robert J. Levine - 1995 - Encyclopedia of Bioethics 3:2311-2316.
     
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  13.  5
    Uncertainty in Clinical Research.Robert J. Levine - 1988 - Journal of Law, Medicine and Ethics 16 (3-4):174-182.
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  14.  2
    Uncertainty in Clinical Research.Robert J. Levine - 1988 - Journal of Law, Medicine and Ethics 16 (3-4):174-182.
  15. Advice on Compensation: One IRB's Response to DHEW's 'Interim Final Regulation'.Robert J. Levine - 1979 - IRB: Ethics & Human Research 1 (1):5.
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  16. Advice on Compensation: More Responses to DHEW's 'Interim Final Regulation'.Robert J. Levine - 1979 - IRB: Ethics & Human Research 1 (2):5.
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  17. What Should Consent Forms Say About Cash Payments?Robert J. Levine - 1979 - IRB: Ethics & Human Research 1 (6):7.
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  18.  12
    Commentary.Robert J. Levine - 1991 - Hastings Center Report 21 (2):27-29.
  19.  3
    Ethics and Research on Human Subjects: International Guidelines: Proceedings of the Xxvith Cioms Conference, Geneva, Switzerland, 5-7 February 1992. [REVIEW]Zbigniew Bańkowski & Robert J. Levine (eds.) - 1993 - Cioms.
  20. Development of New Medicines: Ethical Questions : Proceedings of a Conference Sponsored by Foundation Rhône-Poulenc Sauté, Held in Paris, 2 December 1988.Yves Champey, Robert J. Levine & Paul S. Lietman - 1988
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  21. More on Making Consent Forms More Readable.T. M. Grundner, Robert J. Levine & Alan Meisel - 1982 - IRB: Ethics & Human Research 4 (1):8.
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  22. According to Protocol.Robert J. Levine - 1982 - IRB: Ethics & Human Research 4 (6):9.
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  23.  2
    Biomedical Research Ethics: Updating International Guidelines: A Consultation: Geneva, Switzerland, 15-17 March 2000.Robert J. Levine, Samuel Gorovitz & James Gallagher (eds.) - 2000 - Cioms.
    Records the papers and commentaries, with an edited discussion, presented at an international consultation convened by the Council for International Organizations of Medical Sciences (CIOMS) to guide revision of the CIOMS International Ethical Guidelines for Biomedical Research Involving Human Subjects. The Guidelines, first issued in 1982 and then revised in 1993, are being updated and expanded to address a number of new and especially challenging ethical issues. These include issues raised by international collaborative trials of drugs in developing countries, especially (...)
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  24. Changing Federal Regulation of IRBs: The Commission's Recommendations and the FDA's Proposals.Robert J. Levine - 1979 - IRB: Ethics & Human Research 1 (1):1.
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  25. Can (Or Should) the IRB Assume the FDA's Functions at Early Stages of the IND Process?Robert J. Levine - 1981 - IRB: Ethics & Human Research 3 (10):4.
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  26. Consent to Incomplete Disclosure as an Alternative to Deception.Robert J. Levine - 1982 - IRB: Ethics & Human Research 4 (10):9.
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  27. Deceiving Dentists: Health Care Providers as 'Subjects at Risk'.Robert J. Levine - 1979 - IRB: Ethics & Human Research 1 (5):7.
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  28. [How Many Subjects Are Required for a Study?]: Commentary.Robert J. Levine - 1987 - IRB: Ethics & Human Research 9 (5):3.
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  29. Inconsistency and IRBs: Flaws in the Goldman-Katz Study.Robert J. Levine - 1984 - IRB: Ethics & Human Research 6 (1):4.
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  30. Medical Students as Social Scientists: Are There Role Conflicts?Robert J. Levine - 1980 - IRB: Ethics & Human Research 2 (1):6.
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  31. Research Involving Children: An Interpretation of the New Regulations.Robert J. Levine - 1983 - IRB: Ethics & Human Research 5 (4):1.
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  32. Research on Prisoners: Why Not?Robert J. Levine - 1982 - IRB: Ethics & Human Research 4 (5):6.
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  33. RE: Proposed Rule, Protection of Human Subjects; Informed Consent, 21 CFR Part 50, Et Al.," Federal Register," September 21, 1995 [Docket No. 95N-0158]. [REVIEW]Robert J. Levine - forthcoming - IRB: Ethics & Human Research.
     
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  34. [The Doctor's Unproven Beliefs and the Subject's Informed Choice]: Commentary.Robert J. Levine - 1988 - IRB: Ethics & Human Research 10 (3):5.
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  35. The Senate's Proposed Statutory Definition of 'Voluntary and Informed Consent'.Robert J. Levine - 1980 - IRB: Ethics & Human Research 2 (4):8.
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  36. What Kinds of Subjects Can Understand This Protocol?Robert J. Levine - 1984 - IRB: Ethics & Human Research 6 (5):6.
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  37. What Should Subjects Be Told About Withdrawing From a Protocol?Robert J. Levine - 1981 - IRB: Ethics & Human Research 3 (9):9.
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  38. What Are the IRB's Obligations to Review the Use of Drugs for Purposes That FDA Has Not Approved?Erica Michaels & Robert J. Levine - 1982 - IRB: Ethics & Human Research 4 (4):8.
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  39. Commentary: On Being Queasy.David H. Smith & Robert J. Levine - 1980 - IRB: Ethics & Human Research 2 (4):6.
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  40.  22
    Case Studies: Can a Healthy Subject Volunteer to Be Injured in Research?Anthony Breuer, Robert J. Levine, George A. Kanoti & Douglas P. Lackey - 1986 - Hastings Center Report 16 (4):31.
  41.  8
    FDA's New Rule on Treatment Use and Sale of Investigational New Drugs.Robert J. Levine - 1987 - IRB: Ethics & Human Research 9 (4):1.
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  42.  6
    Commentary: The IRB and the Virtuous Investigator.Robert J. Levine - 1985 - IRB: Ethics & Human Research 7 (1):8.
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  43.  27
    [The Doctor's Unproven Beliefs and the Subject's Informed Choice: Another Commentary]: Response.Robert J. Levine - 1989 - IRB: Ethics & Human Research 11 (3):9.
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  44.  35
    Response to Open Peer Commentaries on “Social Contexts Influence Ethical Considerations of Research”.Robert J. Levine, Judith B. Gordon, Carolyn M. Mazure, Philip E. Rubin, Barry R. Schaller & John L. Young - 2011 - American Journal of Bioethics 11 (5):W1-W2.
    This article argues that we could improve the design of research protocols by developing an awareness of and a responsiveness to the social contexts of all the actors in the research enterprise, including subjects, investigators, sponsors, and members of the community in which the research will be conducted. “Social context” refers to the settings in which the actors are situated, including, but not limited to, their social, economic, political, cultural, and technological features. The utility of thinking about social contexts is (...)
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  45.  5
    Research That Could Yield Marketable Products From Human Materials: The Problem of Informed Consent.Robert J. Levine - 1985 - IRB: Ethics & Human Research 8 (1):6-7.
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  46. Randomized Clinical Trials: Ethical Considerations.Robert J. Levine - 1999 - Advances in Bioethics 5:113-145.
     
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  47. Demystifying Central Review Boards: Current Options and Future Directions: A Summary Report of Outcomes From "Central IRB Review of Multi-Site Trials," 27-28 October 1998. [REVIEW]Robert J. Levine & Louis Lasagna - 2000 - IRB: Ethics & Human Research 22 (6):1.
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  48.  8
    "Demystifying Central Review Boards: Current Options and Future Directions: A Summary Report of Outcomes From" Central IRB Review of Multi-Site Trials," 27-28 October 1998". [REVIEW]Robert J. Levine & Louis Lasagna - forthcoming - IRB: Ethics & Human Research.
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  49.  8
    Such a Bargain!Robert J. Levine - 1989 - Hastings Center Report 19 (1):45-45.
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  50.  12
    Some Reflections on Postgraduate Medical Ethics Education.Robert J. Levine - 1997 - Ethics and Behavior 7 (1):15 – 26.
    Three goals of teaching medical ethics to physicians are reviewed., Components of a basic course in medical ethics are described with special attention to the roles of case conferences, ethics rounds, and role modeling. Obstacles to teaching ethics are also addressed.
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