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Nanoethics: Old Wine, New Bottles?

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Abstract

This paper reviews the question of whether “nanoethics” should be treated as a special essay in ethics, quite different to bioethics, cyberethics, or neuroethics. Whilst some believe that a fundamental rethinking of our ethics is needed, others conclude that ethics as applied to nanoproducts or to nanomedicine will prove to be largely a case of business as usual. The paper is in four principal parts. In the first part, the basic pattern of ethical argument is set out, a pattern that holds no matter which of the emerging technologies is under debate. In the second part, a sketch is offered of the way in which precautionary reasoning plays relative to three key ethical constituencies (utilitarian, rights-led, and dignitarian), including some reflections on how these constituencies would view the so-called precautionary principle (as a guide to regulators). In the third part, the essential features of a particular kind of ethical community, (a “community of rights”) are outlined, such a community being put forward as the appropriate setting for debating matters of nanorisk and regulation. In such a community, the protection of rights is focal, ethics and regulation are viewed as deeply connected discourses, and the aspiration is to develop regimes of control and compensation that are fully integrated and coherent. Finally, there is a discussion of the way in which this kind of community, with its rights-led approach to precaution, would address questions concerning liability for nanoproducts and nanomedical services in a context of profound uncertainty.

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Notes

  1. In general, see Brent Blackwelder (2007). According to Wardak and Gorman (2006), there are already more than 200 nanotechnology-based products in the consumer marketplace, and, more recently, the Royal Commission on Environmental Protection (2008) puts the figure at more than 600.

  2. See Lin (2007; for the view that US regulatory provisions are inadequate), Giorgia Guerra (2008; for the view that European Commission (EC) regulation does not fit very well with potential nanomedical applications), and, generally, Phelps (2007).

  3. Brownsword (2008a). See, too, Brownsword (2008b).

  4. Compare Holm (2005).

  5. Of the emerging technologies, it is neurotechnology rather than nanotechnology that seems most likely to destabilize our self-understanding as agents; but nanotechnology (particularly in conditions of convergence) might destabilize the division between agent subjects and technological objects.

  6. Reno v ACLU 521 US 844 (1997). For regulatory purposes, is the Internet to be viewed as akin to “a library, a telephone, a public park, a local bar, a shopping mall, a broadcast medium, a print medium, a medical clinic, a private living room, [or] a public educational institution[?]”, see Biegel (2001).

  7. Compare Dupuy (2007).

  8. Compare Brownsword (2009).

  9. See Weckert and Moor (2007).

  10. See Yusuf (2007).

  11. UNESCO Universal Declaration on Bioethics and Human Rights (adopted by acclamation on 19 October 2005 by the 33rd session of the General Conference), Article 1.

  12. Compare Spinello (2006). Spinello employs three ethical approaches (utilitarian, contractarian rights-based, and Kantian duty-based), in conjunction with a post-Lessig range of regulatory options, to review four key issues, namely freedom of on-line expression, intellectual property in cyberspace, Internet privacy, and security.

  13. See Klang and Murray (2005).

  14. Compare, Department of Biotechnology, Ministry of Science and Technology, Government of India, National Biotechnology Development Strategy (2006) at 23: “A precautionary, yet promotional approach should be adopted in employing transgenic R & D activities based on technological feasibility, socio-economic considerations and promotion of trade.”

  15. See, further, Brownsword (2007a).

  16. For an excellent discussion, see Stewart (2002).

  17. Moreover, in societies where the trajectory is pro-technology, the precautionary principle is unlikely to be interpreted in a way that does more than slow down the pace of change: see the insightful analysis by van den Daele (2007).

  18. OJ EPO 10/1992, 590.

  19. For discussion of this issue in the context of supposedly “dangerous” offenders, see Bottoms and Brownsword (1983) and Bottoms and Brownsword (1982).

  20. Compare the interesting discussion in Baylis and Fenton (2007).

  21. Compare the analysis in Beyleveld and Brownsword (2001), especially Chapter 6.

  22. For cultural conservativism masquerading as risk analysis, see again Wolfgang van den Daele (2007).

  23. See Brownsword (2005a).

  24. See, e.g., Marchant and Sylvester (2006).

  25. For a more specific elaboration, see Pfizer [2002] ECR II-3305, at para 143: “a preventive measure cannot properly be based on a purely hypothetical approach to risk, founded on mere conjecture which has not been scientifically verified.” So, mere conjecture and hypothesis will not suffice. But, a precautionary measure may apply where the risk “has not yet been fully demonstrated” (para 146). The underlying science must be consistent with principles of “excellence, transparency and independence” (para 172).

  26. See, further, Beyleveld and Brownsword (2009).

  27. According to Weckert and Moor (2007, p. 144), a plausible version of the precautionary principle provides as follows: “If an action A poses a credible threat P of causing some serious harm E, then apply an appropriate remedy R to reduce the possibility of E.” This version still leaves scope for interpretation in relation to the requirements of credibility and seriousness, and the qualifier “appropriate” cues in judgments of proportionality.

  28. The best deep defence of the benchmark involves teasing out the implications of viewing ourselves as agents (with the capacity to engage in practical reason). Seminally, see Gewirth (1978) and Gewirth (1996).

  29. See, further, Brownsword (2005b, 2006).

  30. On will and interest theories of rights, see Hart (1973) and MacCormick (1977).

  31. Compare Beyleveld and Brownsword (2006).

  32. See, further, Brownsword (2004) and Beyleveld and Brownsword (2007).

  33. Compare Beyleveld and Pattinson (2002).

  34. See, further, e.g., Brownsword (2007b).

  35. Compare Blackwelder (2007).

  36. See Farrelly (2007).

  37. Compare the helpful discussion in Weckert and Moor (2007), especially at pp. 140–141.

  38. Compare Farrelly (2007), especially at pp. 220–222.

  39. Compare Mandel (2008).

  40. Compare Dupuy (2007).

  41. This is a strong theme in the Royal Commission on Environmental Protection (2008).

  42. See McHale (2008).

  43. But see van den Hoven (2007).

  44. See, e.g., Harris (2007); and Sandel (2007).

  45. European Group on Ethics in Science and New Technologies to the European Commission (2007) at para 4.1.

  46. European Group on Ethics in Science and New Technologies to the European Commission (2007) at para 5.7.

  47. O’Neill (2003)—a point that is repeated in Manson and O’Neill (2007).

  48. See Brownsword (2008a, Chapter 3).

  49. Compare Mandel (2008).

  50. Compare Noah (2000).

  51. The focal legal provision for the conduct of research trials is Directive 2001/20/EC (the Clinical Trials Directive) but this is part of a larger network of regulation, including Directive 93/42/EEC (on medical devices), Directive 2001/83/EC (on medicinal products for human use), and, most recently, the Advanced Therapies Medicinal Products Regulation (1394/2007/EC).

  52. This, of course, should not be taken as implying that I think that such an evaluation of existing regulation (and the associated processes of review and approval) is unimportant. For relevant discussions, see, e.g., van Calster and Bowman (2008) and Dorbeck-Jung (Dorbeck-Jung 2008).

  53. But, for a different assessment, see, e.g., Goldsmith (1998).

  54. Notably, see Lessig (2001, 2006) and Reidenberg (1998).

  55. For a helpful review, see Deibert and Villeneuve (2005).

  56. See, further, Brownsword (2008a, Chapter 3).

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Brownsword, R. Nanoethics: Old Wine, New Bottles?. J Consum Policy 32, 355–379 (2009). https://doi.org/10.1007/s10603-009-9100-2

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