Literature DB >> 17601870

Participation in biomedical research is an imperfect moral duty: a response to John Harris.

Sandra Shapshay1, Kenneth D Pimple.   

Abstract

In his paper "Scientific research is a moral duty", John Harris argues that individuals have a moral duty to participate in biomedical research by volunteering as research subjects. He supports his claim with reference to what he calls the principle of beneficence as embodied in the "rule of rescue" (the moral obligation to prevent serious harm), and the principle of fairness embodied in the prohibition on "free riding" (we are obliged to share the sacrifices that make possible social practices from which we benefit). His view that biomedical research is an important social good is agreed upon, but it is argued that Harris succeeds only in showing that such participation and support is a moral good, among many other moral goods, while failing to show that there is a moral duty to participate in biomedical research in particular. The flaws in Harris's arguments are detailed here, and it is shown that the principles of beneficence and fairness yield only a weaker discretionary or imperfect obligation to help others in need and to reciprocate for sacrifices that others have made for the public good. This obligation is discretionary in the sense that the individuals are free to choose when, where, and how to help others in need and reciprocate for earlier sacrifices. That Harris has not succeeded in claiming a special status for biomedical research among all other social goods is shown here.

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Year:  2007        PMID: 17601870      PMCID: PMC2598131          DOI: 10.1136/jme.2006.017384

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  3 in total

1.  Responsibilities for poverty-related ill health.

Authors:  Thomas W Pogge
Journal:  Ethics Int Aff       Date:  2002

2.  Scientific research is a moral duty.

Authors:  John Harris
Journal:  J Med Ethics       Date:  2005-04       Impact factor: 2.903

3.  World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects.

Authors: 
Journal:  J Int Bioethique       Date:  2004-03
  3 in total
  7 in total

1.  Viewing research participation as a moral obligation: in whose interests?

Authors:  Stuart Rennie
Journal:  Hastings Cent Rep       Date:  2011 Mar-Apr       Impact factor: 2.683

2.  Withdrawal from biobank research: considerations and the way forward.

Authors:  Kristina Hug; Göran Hermerén; Mats Johansson
Journal:  Stem Cell Rev Rep       Date:  2012-12       Impact factor: 5.739

3.  Inclusion of residual tissue in biobanks: opt-in or opt-out?

Authors:  Noor A A Giesbertz; Annelien L Bredenoord; Johannes J M van Delden
Journal:  PLoS Biol       Date:  2012-08-07       Impact factor: 8.029

4.  When is informed consent required in cluster randomized trials in health research?

Authors:  Andrew D McRae; Charles Weijer; Ariella Binik; Jeremy M Grimshaw; Robert Boruch; Jamie C Brehaut; Allan Donner; Martin P Eccles; Raphael Saginur; Angela White; Monica Taljaard
Journal:  Trials       Date:  2011-09-09       Impact factor: 2.279

5.  The ethics of unlinked anonymous testing of blood: views from in-depth interviews with key informants in four countries.

Authors:  Anthony S Kessel; Jessica Datta; Kaye Wellings; Sarah Perman
Journal:  BMJ Open       Date:  2012-12-20       Impact factor: 2.692

6.  Child's objection to non-beneficial research: capacity and distress based models.

Authors:  Marcin Waligora; Joanna Różyńska; Jan Piasecki
Journal:  Med Health Care Philos       Date:  2016-03

7.  Research Translation and Emerging Health Technologies: Synthetic Biology and Beyond.

Authors:  Sarah Chan
Journal:  Health Care Anal       Date:  2018-12
  7 in total

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