Patient in control in clinical trials - European initiatives for improving patient empowerment in clinical trials through technical implementation of legal norms
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[1] B Hofmann,et al. Broadening consent—and diluting ethics? , 2009, Journal of Medical Ethics.
[2] D. Schillinger,et al. Interventions to Improve Patient Comprehension in Informed Consent for Medical and Surgical Procedures , 2011, Medical decision making : an international journal of the Society for Medical Decision Making.
[3] A. Leach,et al. Making consent patient centred , 2003, BMJ : British Medical Journal.
[4] Peter Singleton,et al. Consent for the use of personal medical data in research , 2006, BMJ : British Medical Journal.
[5] A Cuschieri,et al. Factors affecting quality of informed consent. , 1993, BMJ.
[6] W. Otten,et al. E-health applications and services for patient empowerment: directions for best practices in The Netherlands. , 2010, Telemedicine journal and e-health : the official journal of the American Telemedicine Association.
[7] Sean Cordell,et al. The Ethics of Biobanking: Key Issues and Controversies , 2011, Health Care Analysis.
[8] Carleton B. Chapman,et al. Life and death: philosophical essays in biomedical ethics , 1994, Medical History.
[9] R. Simes,et al. Randomised comparison of procedures for obtaining informed consent in clinical trials of treatment for cancer. , 1986, British medical journal.
[10] Kelly Edwards,et al. From patients to partners: participant-centric initiatives in biomedical research , 2012, Nature Reviews Genetics.