Ethics and Regulation of Clinical Research (Paperback)

Robert J. Levine

ISBN 10: 0300042884 ISBN 13: 9780300042887
Editorial: Yale University Press, New Haven, 1988
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Descripción:

Paperback. The use of human subjects in medical and scientific research has given rise to troubling ethical questions. How should human subjects be selected for experiments? What should they be told about the research in which they are involved? How can their privacy be protected? When is it permissible to deceive them? How do we deal with subjects such as children, fetuses, and the mentally infirm, for whom informed consent is impossible? In this book, Dr. Robert J. Levine reviews federal regulations, ethical analysis, and case studies in an attempt to answer these questions. His book is an essential reference for everyonemembers of institutional review boards, scientists, philosophers, lawyersaddressing the ethical issues involved.[Levines] experience as a clinician, IRB chairman, writer and editor of a journal devoted exclusively to issues faced by IRBS makes him uniquely qualified to bring together the legal, ethical, and practical dimensions. . . [The book] is sophisticated but readable. . . [and] should be on every IRB administrators desk and in every medical ethics library.Norman Fost, M.D., The New England Journal of MedicineLevine. . . is one of the foremost historians of contemporary clinical science. . . . His book is at once a guide to primary sources for the history of clinical research in the late twentieth century and a pioneering secondary source about that history.Daniel M. Fox, Bulletin of the History of MedicineYou will be charmed by the [books] elegance and lucidity and. . . persuaded of its relevance to doctors in any country.Alex Paton, British Medical JournalShould be of wide interest to those keen to see advances in medical research brought into general medical practice.Gilbert Omenn, Issues in Science and Technology The use of human subjects in medical and scientific research has given rise to troubling ethical questions. How should human subjects be selected for experiments? What should they be told about the research in which they are involved? How can their privacy be protected? When is it permissible to deceive them? How do we deal with subjects such as children, fetuses, and the mentally infirm, for whom informed consent is impossible? In this book, Dr. Robert J. Levine reviews federal regulations, ethical analysis, and case studies in an attempt to answer these questions. His book is an essential reference for everyone-members of institutional review boards, scientists, philosophers, lawyers-addressing the ethical issues involved. "[Levine's] experience as a clinician, IRB chairman, writer and editor of a journal devoted exclusively to issues faced by IRBS makes him uniquely qualified to bring together the legal, ethical, and practical dimensions.[The book] is sophisticated but readable.[and] should be on every IRB administrator's desk and in every medical ethics library."-Norman Fost, M.D., The New England Journal of Medicine "Levine.is one of the foremost historians of contemporary clinical science. .His book is at once a guide to primary sources for the history of clinical research in the late twentieth century and a pioneering secondary source about that history."-Daniel M. Fox, Bulletin of the History of Medicine "You will be charmed by the [book's] elegance and lucidity and.persuaded of its relevance to doctors in any country."-Alex Paton, British Medical Journal "Should be of wide interest to those keen to see advances in medical research brought into general medical practice."-Gilbert Omenn, Issues in Science and Technology Shipping may be from multiple locations in the US or from the UK, depending on stock availability. N° de ref. del artículo 9780300042887

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Sinopsis:

The use of human subjects in medical and scientific research has given rise to troubling ethical questions. How should human subjects be selected for experiments? What should they be told about the research in which they are involved? How can their privacy be protected? When is it permissible to deceive them? How do we deal with subjects such as children, fetuses, and the mentally infirm, for whom informed consent is impossible? In this book, Dr. Robert J. Levine reviews federal regulations, ethical analysis, and case studies in an attempt to answer these questions. His book is an essential reference for everyone-members of institutional review boards, scientists, philosophers, lawyers-addressing the ethical issues involved. "[Levine's] experience as a clinician, IRB chairman, writer and editor of a journal devoted exclusively to issues faced by IRBS makes him uniquely qualified to bring together the legal, ethical, and practical dimensions. . . [The book] is sophisticated but readable. . . [and] should be on every IRB administrator's desk and in every medical ethics library."-Norman Fost, M.D., The New England Journal of Medicine "Levine. . . is one of the foremost historians of contemporary clinical science. . . . His book is at once a guide to primary sources for the history of clinical research in the late twentieth century and a pioneering secondary source about that history."-Daniel M. Fox, Bulletin of the History of Medicine "You will be charmed by the [book's] elegance and lucidity and. . . persuaded of its relevance to doctors in any country."-Alex Paton, British Medical Journal "Should be of wide interest to those keen to see advances in medical research brought into general medical practice."-Gilbert Omenn, Issues in Science and Technology

Acerca del autor: Charlotte y Peter Fiell son dos autoridades en historia, teoría y crítica del diseño y han escrito más de sesenta libros sobre la materia, muchos de los cuales se han convertido en éxitos de ventas. También han impartido conferencias y cursos como profesores invitados, han comisariado exposiciones y asesorado a fabricantes, museos, salas de subastas y grandes coleccionistas privados de todo el mundo. Los Fiell han escrito numerosos libros para TASCHEN, entre los que se incluyen 1000 Chairs, Diseño del siglo XX, El diseño industrial de la A a la Z, Scandinavian Design y Diseño del siglo XXI.

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Detalles bibliográficos

Título: Ethics and Regulation of Clinical Research (...
Editorial: Yale University Press, New Haven
Año de publicación: 1988
Encuadernación: Paperback
Condición: new
Edición: 2ª Edición

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