David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
Learn more about PhilPapers
Journal of Medical Ethics 38 (10):626-629 (2012)
It is widely agreed that medical researchers who conduct studies in low- and middle-income countries (LMICs) are morally required to ensure that their research benefits the broader host community, not only the subjects. The justification for this moral requirement has not been adequately examined. Most attempts to justify this requirement focus on researchers' interaction with the community as a whole, not on their relationship with their subjects. This paper argues that in some cases, research must benefit the broader host community for researchers to treat subjects and prospective subjects ethically. If research presents substantial net risks to subjects, researchers can ethically ask LMIC citizens to participate only if people in LMICs, normally including people in the host community, stand to benefit
|Keywords||No keywords specified (fix it)|
|Categories||categorize this paper)|
Setup an account with your affiliations in order to access resources via your University's proxy server
Configure custom proxy (use this if your affiliation does not provide a proxy)
|Through your library|
References found in this work BETA
No references found.
Citations of this work BETA
No citations found.
Similar books and articles
Robert C. Hughes (2014). Justifying Community Benefit Requirements in International Research. Bioethics 28 (8):397-404.
Bernice S. Elger (2008). Research Involving Prisoners: Consensus and Controversies in International and European Regulations. Bioethics 22 (4):224–238.
Eric Chwang (2010). Against Risk-Benefit Review of Prisoner Research. Bioethics 24 (1):14-22.
Alex Rajczi (2004). Making Risk-Benefit Assessments of Medical Research Protocols. Journal of Law, Medicine and Ethics 32 (2):338-348.
Janet Malek (2007). Understanding Risks and Benefits in Research on Reproductive Genetic Technologies. Journal of Medicine and Philosophy 32 (4):339 – 358.
Annette Rid & David Wendler (2011). A Framework for Risk-Benefit Evaluations in Biomedical Research. Kennedy Institute of Ethics Journal 21 (2):141-179.
Sonja Grover (2003). On the Limits of Parental Proxy Consent: Children's Right to Non-Participation in Non-Therapeutic Research. [REVIEW] Journal of Academic Ethics 1 (4):349-383.
Gillian Nycum & Lynette Reid (2007). The Harm-Benefit Tradeoff in "Bad Deal" Trials. Kennedy Institute of Ethics Journal 17 (4):321-350.
Robert Sparrow (2009). Xenotransplantation, Consent and International Justice. Developing World Bioethics 9 (3):119-127.
Elisabeth Weisser-Lohmann (2012). Ethical Aspects of Vulnerability in Research. Poiesis and Praxis 9 (1-2):157-162.
A. Salama, K. Anderson & J. S. Toms (2011). Does Community and Environmental Responsibility Affect Firm Risk? Evidence From UK Panel Data 1994–2006. Business Ethics 20 (2):192-204.
Alan Wertheimer (2013). Is Payment a Benefit? Bioethics 27 (2):105-116.
Denise Chrysler, Harry McGee, Janice Bach, Ed Goldman & Peter D. Jacobson (2011). The Michigan BioTrust for Health: Using Dried Bloodspots for Research to Benefit the Community While Respecting the Individual. Journal of Law, Medicine and Ethics 39 (s1):98-101.
Emmanuelle Lévesque, Yann Joly & Jacques Simard (2011). Return of Research Results: General Principles and International Perspectives. Journal of Law, Medicine and Ethics 39 (4):583-592.
Added to index2012-05-06
Total downloads8 ( #182,604 of 1,168,037 )
Recent downloads (6 months)1 ( #140,420 of 1,168,037 )
How can I increase my downloads?