- History of Clinical Research and Ethics.Shamima Parvin Lasker - 2013 - Bangladesh Journal of Bioethics 4 (1):20-29.details
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The Social Value of Knowledge and International Clinical Research.Danielle M. Wenner - 2013 - Developing World Bioethics 15 (2):76-84.details
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Ethical Concerns Regarding Operations by Volunteer Surgeons on Vulnerable Patient Groups: The Case of Women with Obstetric Fistulas. [REVIEW]L. Lewis Wall - 2011 - HEC Forum 23 (2):115-127.details
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Inducing HIV Remission in Neonates: Child Rights and Research Ethics.Katherine Wade & Armand H. Matheny Antommaria - 2015 - Perspectives in Biology and Medicine 58 (3):348-354.details
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Implications of the concept of minimal risk in research on informed choice in clinical practice.Kyoko Wada & Jeff Nisker - 2015 - Journal of Medical Ethics 41 (10):804-808.details
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A qualitative study using traditional community assemblies to investigate community perspectives on informed consent and research participation in western Kenya.Rachel Vreeman, Eunice Kamaara, Allan Kamanda, David Ayuku, Winstone Nyandiko, Lukoye Atwoli, Samuel Ayaya, Peter Gisore, Michael Scanlon & Paula Braitstein - 2012 - BMC Medical Ethics 13 (1):23-.details
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Legislative regulation and ethical governance of medical research in different European Union countries.Piret Veerus, Joel Lexchin & Elina Hemminki - 2014 - Journal of Medical Ethics 40 (6):409-413.details
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What is the best standard for the standard of care in clinical research?Rieke van der Graaf & Johannes J. M. van Delden - 2009 - American Journal of Bioethics 9 (3):35 – 43.details
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Understandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.Karim Traore, Susan Bull, Alassane Niare, Salimata Konate, Mahamadou A. Thera, Dominic Kwiatkowski, Michael Parker & Ogobara K. Doumbo - 2015 - BMC Medical Ethics 16 (1):1-10.details
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Review of Legal Instruments and Codes on Medical Experimentation with Children. [REVIEW]Sujit Choudhry - 1994 - Cambridge Quarterly of Healthcare Ethics 3 (4):560.details
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Research Guideline Recommendations for Broad Consent Forms in Biobank Research and How They Are Currently Addressed in Practice.Daniel Strech, Hannes Kahrass & Irene Hirschberg - 2015 - American Journal of Bioethics 15 (9):60-63.details
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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.N. Sofaer, C. Thiessen, S. D. Goold, J. Ballou, K. A. Getz, G. Koski, R. A. Krueger & J. S. Weissman - 2009 - Journal of Medical Ethics 35 (3):183-188.details
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Ethical Theories Used by Neurosurgery Residents to Make Decisions in Challenging Cases of Medical Ethics.Sahar Sobhani, Anoosheh Ghasemian, Farshad Farzadfar, Hosein Mashhadinejad & Bahram Hejrani - 2016 - Neuroethics 9 (3):253-261.details
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Stem cell tourism in South Africa: The legal position.M. Nothling Slabbert & S. Mahomed - 2012 - South African Journal of Bioethics and Law 5 (2).details
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Ethical principles and placebo-controlled trials – interpretation and implementation of the Declaration of Helsinki’s placebo paragraph in medical research.Antonia-Sophie Skierka & Karin B. Michels - 2018 - BMC Medical Ethics 19 (1):24.details
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Results of a self-assessment tool to assess the operational characteristics of research ethics committees in low- and middle-income countries.Henry Silverman, Hany Sleem, Keymanthri Moodley, Nandini Kumar, Sudeshni Naidoo, Thilakavathi Subramanian, Rola Jaafar & Malini Moni - 2015 - Journal of Medical Ethics 41 (4):332-337.details
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The medical student global health experience: professionalism and ethical implications.S. Shah & T. Wu - 2008 - Journal of Medical Ethics 34 (5):375-378.details
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“You Don't Know Me, But …”: Access to Patient Data and Subject Recruitment in Human Subjects Research.Toby Schonfeld, Joseph S. Brown, N. Jean Amoura & Bruce Gordon - 2011 - American Journal of Bioethics 11 (11):31-38.details
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The Right to Withdraw from Research.G. Owen Schaefer & Alan Wertheimer - 2010 - Kennedy Institute of Ethics Journal 20 (4):329-352.details
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The need for donor consent in mitochondrial replacement.G. Owen Schaefer - 2018 - Journal of Medical Ethics 44 (12):825-829.details
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Emergency research without consent under polish law.Joanna Różyńska & Marek Czarkowski - 2007 - Science and Engineering Ethics 13 (3):337-350.details
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Justifying Public Health Surveillance: Basic Interests, Unreasonable Exercise, and Privacy.Alan Rubel - 2012 - Kennedy Institute of Ethics Journal 22 (1):1-33.details
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Setting risk thresholds in biomedical research: lessons from the debate about minimal risk.Annette Rid - 2014 - Monash Bioethics Review 32 (1-2):63-85.details
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Paternalism and Utilitarianism in Research with Human Participants.David B. Resnik - 2012 - Health Care Analysis (1):1-13.details
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Limits on risks for healthy volunteers in biomedical research.David B. Resnik - 2012 - Theoretical Medicine and Bioethics 33 (2):137-149.details
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Survey on Using Ethical Principles in Environmental Field Research with Place-Based Communities.Dianne Quigley, Alana Levine, David A. Sonnenfeld, Phil Brown, Qing Tian & Xiaofan Wei - 2019 - Science and Engineering Ethics 25 (2):477-517.details
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Closing the translation gap for justice requirements in international research.Bridget Pratt, Deborah Zion, Khin Maung Lwin, Phaik Yeong Cheah, Francois Nosten & Bebe Loff - 2012 - Journal of Medical Ethics 38 (9):552-558.details
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Non-beneficial pediatric research: individual and social interests.Jan Piasecki, Marcin Waligora & Vilius Dranseika - 2015 - Medicine, Health Care and Philosophy 18 (1):103-112.details
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Universal and uniform protection of human subjects in research: Also a fallacy in some developing countries.Delia Outomuro - 2008 - American Journal of Bioethics 8 (11):19 – 20.details
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Compensation of subjects for participation in biomedical research in resource – limited settings: a discussion of practices in Malawi.Wongani Nyangulu, Randy Mungwira, Nginanche Nampota, Osward Nyirenda, Lufina Tsirizani, Edson Mwinjiwa & Titus Divala - 2019 - BMC Medical Ethics 20 (1):1-5.details
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Readiness of ethics review systems for a changing public health landscape in the WHO African Region.Marion Motari, Martin Okechukwu Ota & Joses Muthuri Kirigia - 2015 - BMC Medical Ethics 16 (1):1-9.details
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The job of ‘ethics committees’.Andrew Moore & Andrew Donnelly - 2018 - Journal of Medical Ethics 44 (7):481-487.details
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Health Research Ethics Committees in South Africa 12 years into democracy.Myer Landon & Moodley Keymanthri - 2007 - BMC Medical Ethics 8 (1):1-8.details
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Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya.M. Mlamba Albert, M. Kamuya Dorcas, M. Marsh Vicki, N. Williams Thomas & S. Molyneux Sassy - 2010 - BMC Medical Ethics 11 (1):13.details
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Maintaining respect and fairness in the usage of stored shared specimens.Takafira Mduluza, Nicholas Midzi, Donold Duruza & Paul Ndebele - 2013 - BMC Medical Ethics 14 (S1):S7.details
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Study participants incentives, compensation and reimbursement in resource-constrained settings.Takafira Mduluza, Nicholas Midzi, Donold Duruza & Paul Ndebele - 2013 - BMC Medical Ethics 14 (S1):S4.details
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Ethical considerations for research involving pregnant women living with HIV and their young children: a systematic review of the empiric literature and discussion.Megan S. McHenry, Mary A. Ott, Elizabeth C. Whipple, Katherine R. MacDonald, Leslie A. Enane & Catherine G. Raciti - 2021 - BMC Medical Ethics 22 (1):1-18.details
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Routine third party disclosure of hiv results to identifiable sexual partners in sub-Saharan Africa.Francis Masiye & Robert Ssekubugu - 2008 - Theoretical Medicine and Bioethics 29 (5):341-348.details
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Post‐trial obligations in the Declaration of Helsinki 2013: classification, reconstruction and interpretation.Ignacio Mastroleo - 2016 - Developing World Bioethics 16 (2):80-90.details
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“I passed the test!” Evidence of diagnostic misconception in the recruitment of population controls for an H3Africa genomic study in Cape Town, South Africa.Francis Masiye, Bongani Mayosi & Jantina de Vries - 2017 - BMC Medical Ethics 18 (1):12.details
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Who should decide about children’s and adolescents’ participation in health research? The views of children and adults in rural Kenya.Vicki Marsh, Nancy Mwangome, Irene Jao, Katharine Wright, Sassy Molyneux & Alun Davies - 2019 - BMC Medical Ethics 20 (1):41.details
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Protecting communities in biomedical research.Patricia A. Marshall & Jessica W. Berg - 2006 - American Journal of Bioethics 6 (3):28 – 30.details
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Human rights,cultural pluralism, and international health research.Patricia A. Marshall - 2005 - Theoretical Medicine and Bioethics 26 (6):529-557.details
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Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya.V. M. Marsh, D. M. Kamuya, A. M. Mlamba, T. N. Williams & S. S. Molyneux - 2010 - BMC Medical Ethics 11 (1):13-13.details
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Evaluating community engagement in global health research: the need for metrics.Kathleen M. MacQueen, Anant Bhan, Janet Frohlich, Jessica Holzer & Jeremy Sugarman - 2015 - BMC Medical Ethics 16 (1):1-9.details
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Ethical challenges in HIV microbicide research: What protections do women need?Ruth Macklin - 2011 - International Journal of Feminist Approaches to Bioethics 4 (2):124-143.details
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Research Ethics. The Good Practices.M. ª Teresa López de la Vieja - 2008 - Arbor 184 (730).details
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Modelos para la investigación con embriones.M. ª Teresa López de la Vieja - 2013 - Arbor 189 (763):a066.details
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Ethical Tradeoffs in Trial Design: Case Study of an HPV Vaccine Trial in HIV‐Infected Adolescent Girls in Lower Income Settings.J. C. Lindsey, S. K. Shah, G. K. Siberry, P. Jean-Philippe & M. J. Levin - 2013 - Developing World Bioethics 13 (2):95-104.details
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Avoiding a jekyll-and-Hyde approach to the ethics of clinical research and practice.Trudo Lemmens & Paul B. Miller - 2002 - American Journal of Bioethics 2 (2):14 – 17.details
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