The Ethics of Biomedical Research: An International Perspective
Baruch A. Brody, Leon Jaworski Professor of Biomedical Ethics Director of the Center for Medical Ethics and Health Policy Baruch A Brody
Oxford University Press, 1998 - 386 sider
This book analyzes the major issues of research ethics through a careful review of the treatment in official policies on research ethics developed throughout the world (especially North America, Western Europe, and the Pacific Rim). Among the issues covered are animal research, research on
human subjects, epidemiological research, genetic research, reproductive research, research on vulnerable subjects, clinical trials, drug approval and the research process, and research on women and minorities. Brody also evaluates the content and the methods of developing these policies in light of
his philosophical position of pluralistic casuistry.
This is the only book that analyzes all the major issues in research ethics. It is the only book which deals with these issues from an international perspective rather than just a US perspective. Major official policies from important research-intensive countries are reprinted in the appendix
(close to 200 plates of otherwise difficult material).
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Chapter One The Use of Animals in Research
Chapter Two Research on Human Subjects
Chapter Three Epidemiological Research
Chapter Four Genetic Research
Chapter Five Reproductive and Fetal Research
Chapter Six Research Involving Vulnerable Subjects
Chapter Seven Clinical Trials
Chapter Nine Research Involving Women and Members
Chapter Ten Philosophical Reflections
International Research Ethics Policies
European Transnational Research Ethics Policies
U S Research Ethics Policies
Research Ethics Policies from Other Countries
Acknowledgment of Sources
Chapter Eight Research and the DrugDevice Approval Process
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acceptable activity additional adequate adopted Agency allowed animals Appendix applicable approach appropriate approval authority balancing benefits carried cells Chapter clinical trials committee concerns conducted confidentiality consideration considered continue Council countries decision designed direct discussed disease drug effects embryo emerged ensure epidemiological ethical example existing experiments fetal gene therapy genetic given guidelines harm human subjects identified important independent individual informed consent institution interests intervention issues justified limited means medical research minimal minority moral obtained official policies participation particular patients pediatric person physician position possible potential practice principles problems procedures programs proposed protection protocols question raised reasons receive regulations representative research involving respect response risks safety scientific specified standards sufficient testing therapeutic tissue treatment United values women
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