How clinical trials really work: Rethinking research ethics
Kennedy Institute of Ethics Journal 21 (2):121-139 (2011)
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Debra A. DeBruin, Joan Liaschenko & Anastasia Fisher (2011). How Clinical Trials Really Work Rethinking Research Ethics. Kennedy Institute of Ethics Journal 21 (2).
Maurie Markman (2004). The Research Misconception. International Journal of Applied Philosophy 18 (2):241-252.
Simon Woods & Pauline Mccormack (2013). Disputing the Ethics of Research: The Challenge From Bioethics and Patient Activism to the Interpretation of the Declaration of Helsinki in Clinical Trials. Bioethics 27 (5):243-250.
Margaret B. Liu (2010). A Clinical Trials Manual From the Duke Clinical Research Institute: Lessons From a Horse Named Jim. Wiley-Blackwell.
Danielle Laudy (forthcoming). End of Life Pediatric Research: What About the Ethics? Journal of Academic Ethics.
Joan Box (2004). Placebos and the UK Medical Research Council — and the Consumer Perspective. Science and Engineering Ethics 10 (1).
Marek Czarkowski (2006). The Protection of Patients' Rights in Clinical Trials. Science and Engineering Ethics 12 (1):131-138.
Malcolm G. Booth (2007). Informed Consent in Emergency Research: A Contradiction in Terms. Science and Engineering Ethics 13 (3).
Marcin Waligora (forthcoming). A European Consistency for Functioning of RECs? We Just Lost Our Chance. Journal of Medical Ethics.
Jeremy Sugarman (2004). Using Empirical Data to Inform the Ethical Evaluation of Placebo Controlled Trials. Science and Engineering Ethics 10 (1).
Sergio Sismondo (2009). Medical Research for Hire: The Political Economy of Pharmaceutical Clinical Trials – by Jill A. Fisher When Experiments Travel: Clinical Trials and the Global Search for Human Subjects – by Adriana Petryna. Bioethics 23 (9):522-524.
Sven Ove Hansson (2006). Uncertainty and the Ethics of Clinical Trials. Theoretical Medicine and Bioethics 27 (2):149-167.
Boleslav Lichterman (2002). Conflict or Harmony? Clinical Research and the Medical Press in Russia. Science and Engineering Ethics 8 (3).
Charles Weijer (1999). Selecting Subjects for Participation in Clinical Research: One Sphere of Justice. Journal of Medical Ethics 25 (1):31-36.
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