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Ezekiel J. Emanuel (ed.)
Oxford University Press (2008)
Comprehensive in scope and research, this book will be a crucial resource for researchers in the medical sciences, as well as teachers and students alike.
|Keywords||Human experimentation in medicine Moral and ethical aspects Clinical trials Moral and ethical aspects Medical ethics Human Experimentation ethics Ethics Committees, Research Ethics, Research Research Subjects legislation & jurisprudence|
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|Call number||R853.H8.O96 2008|
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Deryck Beyleveld & Sebastian Sethe, The European Community Directives on Data Protection and Clinical Trials.
D. Brock, E. J. Emanuel, C. Grady, R. Lie, F. Miller & D. Wendler, Philosophical Justifications of Informed Consent in Research.
Joan P. Porter Greg Koski, Regulations for the Protection of Humans in Research in the United States.
J. V. Lavery, The Obligation to Ensure Access to Beneficial Treatments for Research Participants at the Conclusion of Clinical Trials.
Joan P. Porter & Greg Koski, Regulations for the Protection of Humans in Research in the United States.
Donald L. Rosenstein & Franklin G. Miller, Research Involving Those at Risk for Impaired Decision-Making Capacity.
Deryck Beyleveld Sebastian Sethe, The European Community Directives on Data Protection and Clinical Trials.
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Citations of this work BETA
John F. Kilner (2009). An Inclusive Ethics for the Twenty-First Century: Implications for Stem Cell Research. Journal of Religious Ethics 37 (4):683-722.
Frederic Gilbert, Andrej Vranic & Samia Hurst (2013). Involuntary & Voluntary Invasive Brain Surgery: Ethical Issues Related to Acquired Aggressiveness. [REVIEW] Neuroethics 6 (1):115-128.
Christopher Mayes (2012). On the Importance of the Institution and Social Self in a Sociology of Conflicts of Interest. Journal of Bioethical Inquiry (Browse Results) 9 (2):217-218.
Wendy A. Rogers & Jane Johnson (2013). Addressing Within-Role Conflicts of Interest in Surgery. Journal of Bioethical Inquiry 10 (2):219-225.
Jan Helge Solbakk (2011). In the Ruins of Babel: Pitfalls on the Way Toward a Universal Language for Research Ethics and Benefit Sharing. Cambridge Quarterly of Healthcare Ethics 20 (3):341-355.
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