© 2005 BMJ Publishing Group Ltd & Institute of Medical Ethics
CONTROVERSY
Scientific research
Scientific research is a moral duty
Correspondence to:
Correspondence to:
John Harris
john.m.harris@manchester.ac.uk
Biomedical research is so important that there is a positive moral obligation to pursue it and to participate in it
Keywords: scientific research; biomedical research; medical ethics
| The first 150 words of the full text of this article appear below. |
Science is under attack. In Europe, America, and Australasia in particular, scientists are objects of suspicion and are on the defensive.i
"Frankenstein science"58 is a phrase never far from the lips of those who take exception to some aspect of science or indeed some supposed abuse by scientists. We should not, however, forget the powerful obligation there is to undertake, support, and participate in scientific research, particularly biomedical research, and the powerful moral imperative that underpins these obligations. Now it is more imperative than ever to articulate and explain these obligations and to do so is the subject and the object of this paper.
Let me present the question in its starkest form: is there a moral obligation to undertake, support and even to participate in serious scientific research? If there is, does that obligation require not only that beneficial research be undertaken but also that "we", as
This article has been cited by other articles:
-
Ives, J., Draper, H., Damery, S., Wilson, S.
(2009). Do family doctors have an obligation to facilitate research?. Fam Pract
0: cmp045v1-cmp045
[Abstract] [Full Text] -
Schaefer, G. O., Emanuel, E. J., Wertheimer, A.
(2009). The Obligation to Participate in Biomedical Research. JAMA
302: 67-72
[Abstract] [Full Text] -
Draper, H., Wilson, S., Flanagan, S., Ives, J.
(2009). Offering payments, reimbursement and incentives to patients and family doctors to encourage participation in research. Fam Pract
26: 231-238
[Abstract] [Full Text] -
Peddie, V.L., Porter, M., Counsell, C., Caie, L., Pearson, D., Bhattacharya, S.
(2009). 'Not taken in by media hype': how potential donors, recipients and members of the general public perceive stem cell research. Hum Reprod
24: 1106-1113
[Abstract] [Full Text] -
Hultman, C. M., Lindgren, A.-C., Hansson, M. G., Carlstedt-Duke, J., Ritzen, M., Persson, I., Kieler, H.
(2009). Ethical Issues in Cancer Register Follow-Up of Hormone Treatment in Adolescence. Public Health Ethics
2: 30-36
[Abstract] [Full Text] -
Schuklenk, U., Lowry, C.
(2009). Terminal illness and access to Phase 1 experimental agents, surgeries and devices: reviewing the ethical arguments. Br Med Bull
89: 7-22
[Abstract] [Full Text] -
Buchanan, D., Sifunda, S., Naidoo, N., James, S., Reddy, P.
(2008). Assuring Adequate Protections in International Health Research: A Principled Justification and Practical Recommendations for the Role of Community Oversight. Public Health Ethics
1: 246-257
[Abstract] [Full Text] -
Miller, F. G.
(2008). Research on medical records without informed consent.. J Law Med Ethics
36: 560-566
-
Brazier, M
(2008). Exploitation and enrichment: the paradox of medical experimentation. J. Med. Ethics
34: 180-183
[Abstract] [Full Text] -
Draper, H, Ives, J, Parle, J, Ross, N
(2008). Medical education and patients' responsibilities: back to the future?. J. Med. Ethics
34: 116-119
[Abstract] [Full Text] -
Saunders, J.
(2007). More guidelines on research ethics?. J. Med. Ethics
33: 683-684
[Full Text] -
Schmidt, H.
(2007). Patients' charters and health responsibilities. BMJ
0: bmj.39387.393160.ADv1-bmj.39387.393160.AD
[Full Text] -
McGregor, J. L.
(2007). Population Genomics and Research Ethics with Socially Identifable Groups. J Law Med Ethics
35: 356-370
-
Shapshay, S., Pimple, K. D
(2007). Participation in biomedical research is an imperfect moral duty: a response to John Harris. J. Med. Ethics
33: 414-417
[Abstract] [Full Text] -
Ives, J
(2007). Kant, curves and medical learning practice: a reply to Le Morvan and Stock. J. Med. Ethics
33: 119-122
[Abstract] [Full Text] -
Hill, T. P.
(2007). Phase 0 Trials: Are They Ethically Challenged?. Clin. Cancer Res.
13: 783-784
[Full Text] -
Holm, S, Takala, T
(2007). High hopes and automatic escalators: a critique of some new arguments in bioethics. J. Med. Ethics
33: 1-4
[Abstract] [Full Text] -
Green, J.
(2006). The evolving randomised controlled trial in mental health: studying complexity and treatment process. Adv. Psychiatr. Treat.
12: 268-279
[Abstract] [Full Text] -
Stobbart, L., Murtagh, M. J, Louw, S. J, Ford, G. A, Rodgers, H.
(2006). Consent for research in hyperacute stroke.. BMJ
332: 1405-1406
[Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
