- Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience. [REVIEW]P. Tindana, S. Bull, L. Amenga-Etego, J. Vries, R. Aborigo, K. Koram, D. Kwiatkowski & M. Parker - 2012 - BMC Medical Ethics 13 (1):15-15.details
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Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences.Martine C. de Vries, Mirjam Houtlosser, Jan M. Wit, Dirk P. Engberts, Dorine Bresters, Gertjan Jl Kaspers & Evert van Leeuwen - 2011 - BMC Medical Ethics 12 (1):1-11.details
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Seeking consent to genetic and genomic research in a rural Ghanaian setting: A qualitative study of the MalariaGEN experience. [REVIEW]Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski & Michael Parker - 2012 - BMC Medical Ethics 13 (1):15-.details
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Unique ethical concerns in clinical trials comparing psychosocial and psychopharmalogical interventions.Lisa R. Stines & Norah C. Feeny - 2008 - Ethics and Behavior 18 (2-3):234 – 246.details
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Restricted treatments, inducements, and research participation.Sarah J. L. Edwards - 2006 - Bioethics 20 (2):77–91.details
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Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences.C. de Vries Martine, Houtlosser Mirjam, M. Wit Jan, P. Engberts Dirk, Bresters Dorine, J. L. Kaspers Gertjan & van Leeuwen Evert - 2011 - BMC Medical Ethics 12 (1):18.details
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(2 other versions)A Review of: “Jerome P. Kassirer. 2004. On the Take: How Medicine's Complicity with Big Business Can Endanger Your Health”: New York: Oxford University Press. 251 pp. $28.00, hardcover. [REVIEW]Alexander C. Tsai - 2005 - American Journal of Bioethics 5 (2):66-68.details
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When "Minimal Risk" Research Yields Clinically-Significant Data, Maybe the Risks Aren't So Minimal.Helen M. Sharp & Robert D. Orr - 2004 - American Journal of Bioethics 4 (2):32-36.details
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(1 other version)The Clinical Investigator as Fiduciary: Discarding a Misguided Idea.E. Haavi Morreim - 2005 - Journal of Law, Medicine and Ethics 33 (3):586-598.details
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Informed consent in paediatric critical care research – a South African perspective.Brenda M. Morrow, Andrew C. Argent & Sharon Kling - 2015 - BMC Medical Ethics 16 (1):62.details
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Developing Clinical Research Relationship: Views from Within.Olga Zvonareva & Lloyd Akrong - 2014 - Developing World Bioethics 15 (3):257-266.details
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Accountability and pediatric physician-researchers: are theoretical models compatible with Canadian lived experience?Christine Czoli, Michael Da Silva, Randi Zlotnik Shaul, Lori D'Agincourt-Canning, Christy Simpson, Katherine Boydell, Natalie Rashkovan & Sharon Vanin - 2011 - Philosophy, Ethics, and Humanities in Medicine 6:15.details
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(1 other version)A Review of: “Timothy F. Murphy. 2004. Case Studies in Biomedical Research Ethics”: Cambridge, MA: The MIT Press. 368 pp. $29.00, paperback. [REVIEW]David Rodríguez-Arias & Christian Hervé - 2005 - American Journal of Bioethics 5 (2):64-66.details
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(1 other version)The Clinical Investigator as Fiduciary: Discarding a Misguided Idea.E. Haavi Morreim - 2005 - Journal of Law, Medicine and Ethics 33 (3):586-598.details
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Equipoise may be in the eye of the beholder.Anne Moyer & Anna H. L. Floyd - 2009 - American Journal of Bioethics 9 (2):21 – 22.details
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Different Context, Similar Motives: External Influences on Motivation.Aisha Y. Malik - 2015 - American Journal of Bioethics 15 (11):26-28.details
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Reassessing the Role of the Biomedical Research Ethics Committee.Merryn Ekberg - 2012 - Journal of Academic Ethics 10 (4):335-352.details
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The picture talk project: Aboriginal community input on consent for research.Emily F. M. Fitzpatrick, Gaynor Macdonald, Alexandra L. C. Martiniuk, June Oscar, Heather D’Antoine, Maureen Carter, Tom Lawford & Elizabeth J. Elliott - 2019 - BMC Medical Ethics 20 (1):12.details
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(1 other version)A Review of: “Timothy F. Murphy. 2004. Case Studies in Biomedical Research Ethics”: Cambridge, MA: The MIT Press. 368 pp. $29.00, paperback. [REVIEW]David Rodríguez-Arias & Christian Hervé - 2005 - American Journal of Bioethics 5 (2):64-66.details
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Ethical issues related to computerised family medical histories in sickle cell disease: Inforare.S. Franrenet, N. Duchange, F. Galacteros, C. Quantin, O. Cohen, R. Nzouakou, S. Sudraud, C. Herve & G. Moutel - 2010 - Journal of Medical Ethics 36 (10):604-607.details
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