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  • Cited by 6
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    This article has been cited by the following publications. This list is generated based on data provided by CrossRef.

    Cool, Alison 2015. Detaching data from the state: Biobanking and building Big Data in Sweden. BioSocieties,


    Montelius, Kerstin Stenersen, Marguerethe and Sajantila, Antti 2014. eLS.


    Capps, B. 2012. The Public Interest, Public Goods, and Third-Party Access to UK Biobank. Public Health Ethics, Vol. 5, Issue. 3, p. 240.


    Knoppers, Bartha Maria Zawati, Ma'n H. and Kirby, Emily S. 2012. Sampling Populations of Humans Across the World: ELSI Issues. Annual Review of Genomics and Human Genetics, Vol. 13, Issue. 1, p. 395.


    McCarthy, P. 2012. Encyclopedia of Applied Ethics.


    Malin, Bradley Loukides, Grigorios Benitez, Kathleen and Clayton, Ellen Wright 2011. Identifiability in biobanks: models, measures, and mitigation strategies. Human Genetics, Vol. 130, Issue. 3, p. 383.


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  • Cambridge Quarterly of Healthcare Ethics, Volume 15, Issue 3
  • July 2006, pp. 285-293

Bioethics in Sweden

  • SVEN OVE HANSSON (a1) and BARBRO BJÖRKMAN (a1)
  • DOI: http://dx.doi.org/10.1017/S0963180106060361
  • Published online: 01 July 2006
Abstract

Sweden is probably one of the most secularized nations in the world. Therefore religious arguments tend to play a smaller role in the public bioethical debate than in most other countries. Issues such as abortion, stem-cell research, and therapeutic cloning have been far less controversial in Sweden than elsewhere. Instead, other issues have dominated recent bioethical debates in Sweden, in particular those concerning privacy and the control over biological information about individuals.

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Cambridge Quarterly of Healthcare Ethics
  • ISSN: 0963-1801
  • EISSN: 1469-2147
  • URL: /core/journals/cambridge-quarterly-of-healthcare-ethics
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