Abstract
This chapter includes offers and respective on requirement proportionality today and in the future.
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- 1.
Cf. Section 2.2 and Simonsen (2011); See Judgment by the ECtHR in Bosphorus Hava Yallari Turizm ve Ticaret Anonim Sirketi v. Ireland of 30 June 2009 (Grand Chamber, with dissenting opinion), Paragraph 159.
- 2.
Jonas (1982, cited in Meslin 1989, p. 247).
- 3.
See Chapter 12 concerning clinical trials on persons not able to consent.
References
Meslin, E.M. 1989. Protecting human subjects from harm in medical research: A proposal for improving risk judgments by institutional review boards. Washington, DC: Georgetown University.
Simonsen, S. 2011. European integration: A case-example from biomedical research law. In Nordic anthology of health law. Under publication.
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Simonsen, S. (2012). Perspectives. In: Acceptable Risk in Biomedical Research. International Library of Ethics, Law, and the New Medicine, vol 50. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-2678-9_20
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DOI: https://doi.org/10.1007/978-94-007-2678-9_20
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