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Informed Consent: Practices and Views of Investigators in a Multinational Clinical Trial
Lindsay Sabik, Christine A. Pace, Heidi P. Forster-Gertner, David Wendler, Judith D. Bebchuk, Jorge A. Tavel, Laura A. McNay, Jack Killen, Ezekiel J. Emanuel & Christine Grady
IRB: Ethics & Human Research 27 (5):13-18 (2004)
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Voluntary participation and comprehension of informed consent in a genetic epidemiological study of breast cancer in Nigeria.Patricia A. Marshall, Clement A. Adebamowo, Adebowale A. Adeyemo, Temidayo O. Ogundiran, Teri Strenski, Jie Zhou & Charles N. Rotimi - 2014 - BMC Medical Ethics 15 (1):38.
Can informed consent to research be adapted to risk?Danielle Bromwich & Annette Rid - 2015 - Journal of Medical Ethics 41 (7):521-528.
Post-trial access to study medication: a Brazilian e-survey with major stakeholders in clinical research.Sonia M. Dainesi & Moises Goldbaum - 2012 - Journal of Medical Ethics 38 (12):757-762.
Survey of risks and benefits communication strategies by research nurses.Lika Nusbaum, Brenda Douglas, Neenah Estrella-Luna, Michael Paasche-Orlow & Karla Damus - 2019 - Nursing Ethics 26 (3):937-950.
Informed consent in clinical research in France: assessment and factors associated with therapeutic misconception.I. S. Durand-Zaleski, C. Alberti, P. Durieux, X. Duval, S. Gottot, P. Ravaud, S. Gainotti, C. Vincent-Genod, D. Moreau & P. Amiel - 2008 - Journal of Medical Ethics 34 (9):e16-e16.
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