Information giving in clinical trials: The views of medical researchers
Bioethics 17 (1):101–111 (2003)
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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.
N. Sofaer, C. Thiessen, S. D. Goold, J. Ballou, K. A. Getz, G. Koski, R. A. Krueger & J. S. Weissman (2009). Subjects' Views of Obligations to Ensure Post-Trial Access to Drugs, Care and Information: Qualitative Results From the Experiences of Participants in Clinical Trials (EPIC) Study. Journal of Medical Ethics 35 (3):183-188.
Marek Czarkowski (2006). The Protection of Patients' Rights in Clinical Trials. Science and Engineering Ethics 12 (1):131-138.
Boleslav Lichterman (2002). Conflict or Harmony? Clinical Research and the Medical Press in Russia. Science and Engineering Ethics 8 (3).
Maurie Markman (2004). The Research Misconception. International Journal of Applied Philosophy 18 (2):241-252.
Leslie Cannold (1997). "There Is No Evidence to Suggest...": Changing the Way We Judge Information for Disclosure in the Informed Consent Process. Hypatia 12 (2):165 - 184.
P. R. Ferguson (2002). Patients' Perceptions of Information Provided in Clinical Trials. Journal of Medical Ethics 28 (1):45-48.
Joan Box (2004). Placebos and the UK Medical Research Council — and the Consumer Perspective. Science and Engineering Ethics 10 (1).
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