- Does Consent Bias Research?Mark A. Rothstein & Abigail B. Shoben - 2013 - American Journal of Bioethics 13 (4):27 - 37.details
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Assuring Adequate Protections in International Health Research: A Principled Justification and Practical Recommendations for the Role of Community Oversight.David Buchanan, Sibusiso Sifunda, Nasheen Naidoo, Shamagonam James & Priscilla Reddy - 2008 - Public Health Ethics 1 (3):246-257.details
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A Duty to Participate in Research: Does Social Context Matter?Inmaculada de Melo-Martín - 2008 - American Journal of Bioethics 8 (10):28-36.details
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Haben Patient*innen die moralische Pflicht, ihre klinischen Daten für Forschung bereitzustellen? Eine kritische Prüfung möglicher Gründe.Martin Jungkunz, Anja Köngeter, Katja Mehlis, Markus Spitz, Eva C. Winkler & Christoph Schickhardt - 2022 - Ethik in der Medizin 34 (2):195-220.details
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The Obligation to Participate in Biomedical Research.G. Owen Schaefer, Ezekiel J. Emanuel & Alan Wertheimer - 2009 - Journal of the American Medical Association 302 (1):67-72.details
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The Ethics of Clinical Care and the Ethics of Clinical Research: Yin and Yang.Charles J. Kowalski, Raymond J. Hutchinson & Adam J. Mrdjenovich - 2017 - Journal of Medicine and Philosophy 42 (1):7-32.details
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The Research‐Treatment Distinction: A Problematic Approach for Determining Which Activities Should Have Ethical Oversight.Nancy E. Kass, Ruth R. Faden, Steven N. Goodman, Peter Pronovost, Sean Tunis & Tom L. Beauchamp - 2013 - Hastings Center Report 43 (s1):4-15.details
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Manipulation in the Enrollment of Research Participants.Amulya Mandava & Joseph Millum - 2013 - Hastings Center Report 43 (2):38-47.details
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The fiduciary obligation of the physician-researcher in phase IV trials.Rosemarie Dlc Bernabe, Ghislaine Jmw van Thiel, Jan Am Raaijmakers & Johannes Jm van Delden - 2014 - BMC Medical Ethics 15 (1):11.details
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The Hippocratic Thorn in Bioethics' Hide: Cults, Sects, and Strangeness.T. Koch - 2014 - Journal of Medicine and Philosophy 39 (1):75-88.details
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An Ethics Framework for a Learning Health Care System: A Departure from Traditional Research Ethics and Clinical Ethics.Ruth R. Faden, Nancy E. Kass, Steven N. Goodman, Peter Pronovost, Sean Tunis & Tom L. Beauchamp - 2013 - Hastings Center Report 43 (s1):16-27.details
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Do patients have a moral duty to provide their clinical data for research? A critical examination of possible reasons.Martin Jungkunz, Anja Köngeter, Katja Mehlis, Markus Spitz, Eva C. Winkler & Christoph Schickhardt - 2022 - Ethik in der Medizin 34 (2):195-220.details
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