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Double Standards in Medical Research in Developing Countries

Double Standards in Medical Research in Developing Countries

Double Standards in Medical Research in Developing Countries

Author:
Ruth Macklin, Albert Einstein College of Medicine, New York
Published:
July 2006
Availability:
This ISBN is for an eBook version which is distributed on our behalf by a third party.
Format:
Adobe eBook Reader
ISBN:
9780511208232

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    This book examines the ethical controversies that have surrounded the design and conduct of international medical research sponsored by industrialized countries or industry, and carried out in developing countries. The chief concern is that research subjects in developing countries may be exploited because sponsors of research employ double standards. One debate focuses on whether the standard of care provided to subjects of medical research in developing countries should be the same as what research subjects receive in North America and Europe. Other concerns are whether the process of obtaining informed consent in developing countries is adequate, and whether prior ethical review of research meets standards that are well established in the industrialized world. Recent international developments show that essential medications can be made affordable and accessible to developing countries, and that double standards need not prevail.

    • Presents a detailed account of both sides of recent controversies in international medical research
    • As a member of a committee that revised international ethical guidelines for medical research, the author gives a behind-the-scenes account of the views of many commentators on the guidelines
    • Describes episodes of unethical research sponsored by the pharmaceutical industry and analyses which of these constitute exploitation of research students in developing countries

    Reviews & endorsements

    "The strength of the book lies in its breadth of coverage. It moves from deliberations over the wording of guidelines to theoretical considerations of the substantive content of those words, showing why their careful usage is ethically, and practically salient. Macklin's experience on international committees and study teams adds to the depth of her considerations. [S]he has made an important and timely contribution to the thinking of medical and pharmaceutical professionals, policymakers, and ethicists." Jackie Leach Scully, University of Basel, JAMA

    "The strength of the book lies in its breadth of coverage. It moves from deliberations over the wording of guidelines to theoretical considerations of the substantive content of those words, showing why their careful usage is ethically, and practically salient. Macklin's experience on international committees and study teams adds to the depth of her considerations. [S]he has made an important and timely contribution to the thinking of medical and pharmaceutical professionals, policymakers, and ethicists." Jackie Leach Scully, University of Basel, JAMA

    "[Macklin] has made an important and timely contribution to the thinking of medical and pharmaceutical professionals, poicymakers, and ethicists." JANA

    Product details

    • Published: July 2006
    • Format: Adobe eBook Reader
    • ISBN: 9780511208232
    • Length: 0 pages
    • Weight: 0kg
    • Availability: This ISBN is for an eBook version which is distributed on our behalf by a third party.

    Table of Contents

    • 1. International research contested: controversies and debates
    • 2. Maintaining ethical standards in research
    • 3. Striving for justice in research
    • 4. Avoiding exploitation
    • 5. providing safeguards: informed consent and review of research
    • 6. Making drugs affordable
    • 7. Respecting, protecting, and fulfilling human rights
    • 8. Striving for a single standard
    • Index.

    Author

    Ruth Macklin , Albert Einstein College of Medicine, New York

    Professor of Bioethics, Albert Einstein College of Medicine, New York.