Literature DB >> 18633729

Regulation and the social licence for medical research.

Mary Dixon-Woods1, Richard E Ashcroft.   

Abstract

Regulation and governance of medical research is frequently criticised by researchers. In this paper, we draw on Everett Hughes' concepts of professional licence and professional mandate, and on contemporary sociological theory on risk regulation, to explain the emergence of research governance and the kinds of criticism it receives. We offer explanations for researcher criticism of the rules and practices of research governance, suggesting that these are perceived as interference in their mandate. We argue that, in spite of their complaints, researchers benefit from the institutions of governance and regulation, in particular by the ways in which regulation secures the social licence for research. While it is difficult to answer questions such as: "Is medical research over-regulated?" and "Does the regulation of medical research successfully protect patients or promote ethical conduct?", a close analysis of the social functions of research governance and its relationship to risk, trust, and confidence permits us to pose these questions in a more illuminating way.

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Mesh:

Year:  2008        PMID: 18633729     DOI: 10.1007/s11019-008-9152-0

Source DB:  PubMed          Journal:  Med Health Care Philos        ISSN: 1386-7423


  27 in total

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Authors:  J C Dumville; J Watson; P Raynor; D J Torgerson
Journal:  QJM       Date:  2004-03

3.  Ethics and research governance in a multicentre study: add 150 days to your study protocol.

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Authors:  L Sheard; C N E Tompkins; N M J Wright; C E Adams
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5.  Researchers' responses to research management and governance for primary care research in England: persistent and escalating problems over time.

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Journal:  J Health Organ Manag       Date:  2005

6.  The impact of research governance in the United Kingdom on research involving a national survey.

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Journal:  J Health Organ Manag       Date:  2007

7.  Research governance: impeding both research and teaching? A survey of impact on undergraduate research opportunities.

Authors:  Louise Robinson; Sarah Drewery; John Ellershaw; John Smith; Sue Whittle; Deborah Murdoch-Eaton
Journal:  Med Educ       Date:  2007-08       Impact factor: 6.251

8.  Written work: the social functions of Research Ethics Committee letters.

Authors:  Mary Dixon-Woods; Emma Angell; Richard E Ashcroft; Alan Bryman
Journal:  Soc Sci Med       Date:  2007-05-08       Impact factor: 4.634

9.  The old faith and the new science: the Nuremberg Code and human experimentation ethics in Britain, 1946-73.

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Journal:  Soc Hist Med       Date:  2002-04       Impact factor: 0.973

10.  Ethics and clinical research.

Authors:  H K Beecher
Journal:  N Engl J Med       Date:  1966-06-16       Impact factor: 91.245

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  19 in total

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2.  Legislation, social licence and primate research.

Authors:  I Anna S Olsson; Augusto Vitale
Journal:  EMBO Rep       Date:  2010-01       Impact factor: 8.807

3.  Changes in the institutional review board submission process for multicenter research over 6 years.

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4.  One stop or full stop? The continuing challenges for researchers despite the new streamlined NHS research governance process.

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Journal:  BMC Health Serv Res       Date:  2010-05-13       Impact factor: 2.655

5.  Bioethics and the sociology of trust: introduction to the theme.

Authors:  Raymond G De Vries; Scott Y H Kim
Journal:  Med Health Care Philos       Date:  2008-07-16

6.  A Critical Look at Biomedical Journals' Policies on Animal Research by Use of a Novel Tool: The EXEMPLAR Scale.

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Journal:  Animals (Basel)       Date:  2015-04-30       Impact factor: 2.752

7.  The social licence for research: why care.data ran into trouble.

Authors:  Pam Carter; Graeme T Laurie; Mary Dixon-Woods
Journal:  J Med Ethics       Date:  2015-01-23       Impact factor: 2.903

8.  Governing stem cell therapy in India: regulatory vacuum or jurisdictional ambiguity?

Authors:  Shashank S Tiwari; Sujatha Raman
Journal:  New Genet Soc       Date:  2014-10-29

9.  Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries.

Authors:  Richard Milne; Katherine I Morley; Mohamed A Almarri; Shamim Anwer; Jerome Atutornu; Elena E Baranova; Paul Bevan; Maria Cerezo; Yali Cong; Alessia Costa; Christine Critchley; Josepine Fernow; Peter Goodhand; Qurratulain Hasan; Aiko Hibino; Gry Houeland; Heidi C Howard; S Zakir Hussain; Charlotta Ingvoldstad Malmgren; Vera L Izhevskaya; Aleksandra Jędrzejak; Cao Jinhong; Megumi Kimura; Erika Kleiderman; Brandi Leach; Keying Liu; Deborah Mascalzoni; Álvaro Mendes; Jusaku Minari; Dianne Nicol; Emilia Niemiec; Christine Patch; Jack Pollard; Barbara Prainsack; Marie Rivière; Lauren Robarts; Jonathan Roberts; Virginia Romano; Haytham A Sheerah; James Smith; Alexandra Soulier; Claire Steed; Vigdis Stefànsdóttir; Cornelia Tandre; Adrian Thorogood; Torsten H Voigt; Nan Wang; Anne V West; Go Yoshizawa; Anna Middleton
Journal:  Genome Med       Date:  2021-05-25       Impact factor: 11.117

10.  Creating the 'ethics industry': Mary Warnock, in vitro fertilization and the history of bioethics in Britain.

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Journal:  Biosocieties       Date:  2010-11-29
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