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.
Similar content being viewed by others
Notes
Compare Holm (2005).
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.
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).
Compare Dupuy (2007).
Compare Brownsword (2009).
See Weckert and Moor (2007).
See Yusuf (2007).
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.
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.
See Klang and Murray (2005).
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.”
See, further, Brownsword (2007a).
For an excellent discussion, see Stewart (2002).
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).
OJ EPO 10/1992, 590.
Compare the interesting discussion in Baylis and Fenton (2007).
Compare the analysis in Beyleveld and Brownsword (2001), especially Chapter 6.
For cultural conservativism masquerading as risk analysis, see again Wolfgang van den Daele (2007).
See Brownsword (2005a).
See, e.g., Marchant and Sylvester (2006).
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).
See, further, Beyleveld and Brownsword (2009).
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.
Compare Beyleveld and Brownsword (2006).
Compare Beyleveld and Pattinson (2002).
See, further, e.g., Brownsword (2007b).
Compare Blackwelder (2007).
See Farrelly (2007).
Compare the helpful discussion in Weckert and Moor (2007), especially at pp. 140–141.
Compare Farrelly (2007), especially at pp. 220–222.
Compare Mandel (2008).
Compare Dupuy (2007).
This is a strong theme in the Royal Commission on Environmental Protection (2008).
See McHale (2008).
But see van den Hoven (2007).
European Group on Ethics in Science and New Technologies to the European Commission (2007) at para 4.1.
European Group on Ethics in Science and New Technologies to the European Commission (2007) at para 5.7.
See Brownsword (2008a, Chapter 3).
Compare Mandel (2008).
Compare Noah (2000).
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).
But, for a different assessment, see, e.g., Goldsmith (1998).
For a helpful review, see Deibert and Villeneuve (2005).
See, further, Brownsword (2008a, Chapter 3).
References
Baylis, F., & Fenton, A. (2007). Chimera research and stem cell therapies for human neurodegenerative disorders. Cambridge Quarterly of Healthcare Ethics, 16, 195.
Bazelon, D. L. (1977). Coping with technology through the legal process. Cornell Law Review, 62(817), 826–827.
Beyleveld, D., & Brownsword, R. (2001). Human dignity in bioethics and biolaw. Oxford: Oxford University Press.
Beyleveld, D., & Brownsword, R. (2006). Principle, proceduralism and precaution in a community of rights. Ratio Juris, 19, 141.
Beyleveld, D., & Brownsword, R. (2007). Consent in the law. Oxford: Hart.
Beyleveld, D., & Brownsword, R. (2009). Complex technology, complex calculations: Uses and abuses of precautionary reasoning in law. In M. Duwell & P. Sollie (Eds.), Evaluating new technologies: Methodological problems for the ethical assessment of technological developments (pp. 175–190). New York: Springer.
Beyleveld, D., & Pattinson, S. (2002). Horizontal applicability and direct effect. Law Quarterly Review, 118, 623.
Biegel, S. (2001). Beyond our control? (p. 28). Cambridge, MA: MIT.
Blackwelder, B. (2007). Nanotechnology jumps the gun: Nanoparticles in consumer products. In M. Nigel, S. de Cameron & M. E. Mitchell (Eds.), Nanoscale (p. 71). Hoboken, NJ: Wiley.
Bottoms, A. E., & Brownsword, R. (1982). The dangerousness debate after the Floud report. British Journal of Criminology, 22, 229–254.
Bottoms, A. E., & Brownsword, R. (1983). Dangerousness and rights. In J. Hinton (Ed.), Dangerousness: Problems of assessment and prediction (pp. 9–22). London: Allen and Unwin.
Brownsword, R. (2004). The cult of consent: Fixation and fallacy. King’s College Law Journal, 15, 223.
Brownsword, R. (2005a). Biotechnology and rights: Where are we coming from and where are we going? In M. Klang & A. Murray (Eds.), Human rights in the digital age (p. 219). London: Cavendish.
Brownsword, R. (2005b). Making people better and making better people: Bioethics and the regulation of stem cell research. Journal of Academic Legal Studies, 1, 3.
Brownsword, R. (2006). Cloning, zoning and the harm principle. In S. A. M. McLean (Ed.), First do no harm (p. 527). Aldershot: Ashgate.
Brownsword, R. (2007a). Ethical pluralism and the regulation of modern biotechnology. In F. Francioni (Ed.), The impact of biotechnologies on human rights (p. 45). Oxford: Hart.
Brownsword, R. (2007b). The ancillary care responsibilities of researchers: Reasonable but not great expectations. Journal of Law, Medicine and Ethics, 35, 679–691.
Brownsword, R. (2008a). Rights, regulation and the technological revolution. Oxford: Oxford University Press.
Brownsword, R. (2008b). Regulating nanomedicine—the smallest of our concerns? Nanoethics, 2, 73–86.
Brownsword, R. (2009). Regulating nanotechnologies: A matter of some uncertainty. Politeia (in press)
Davies, J. C. (2006). Managing the effects of nanotechnology. Washington: Woodrow Wilson International Center for Scholars. Available at http://www.wilsoncenter.org/events/docs/Effectsnanotechfinal.pdf (last visited August 30, 2007).
Deibert, R. J., & Villeneuve, N. (2005). Firewalls and power: An overview of global state censorship of the Internet. M. Klang & A. Murray (Eds.), Human rights in the digital age (p. 111). London: Cavendish.
Dorbeck-Jung, B. (2008). How can hybrid nanomedical products regulation cope with wicked governability problems? Presented at the TILT “Tilting Perspectives on Regulating Technologies” Conference, University of Tilburg, December 10 and 11, 2008 (on file with author).
Dupuy, J.-P. (2007). Complexity and uncertainty: A prudential approach to nanotechnology. In F. Allhoff, P. Lin, J. Moor & J. Weckert (Eds.), Nanoethics, Ch. 9 (p. 119). Hoboken, NJ: Wiley.
European Group on Ethics in Science and New Technologies to the European Commission (2007). Opinion on the ethical aspects of nanomedicine (Opinion No 21).
Farrelly, C. (2007). Deliberative democracy and nanotechnology. In F. Allhoff, P. Lin, J. Moor & J. Weckert (Eds.), Nanoethics (pp. 215–216). Hoboken, NJ: Wiley.
Gewirth, A. (1978). Reason and morality. Chicago: University of Chicago Press.
Gewirth, A. (1996). Community of rights. Chicago: University of Chicago Press.
Goldsmith, J. (1998). Against cyberanarchy. University of Chicago Law Review, 65, 1199.
Guerra, G. (2008). European regulatory issues in nanomedicine. Nanoethics, 2, 87.
Harris, J. (2007). Enhancing evolution. Princeton: Princeton University Press.
Hart, H. L. A. (1973). Bentham on legal rights. In A. W. B. Simpson (Ed.), Oxford essays in jurisprudence (second series) (p. 171). Oxford: Clarendon.
Holm, S. (2005). Does nanotechnology require a new ‘nanoethics’?. Wales: CCELS.
Johnson, D. R., & Post, D. (1996). Law and borders—the rise of law in cyberspace. Stanford Law Review, 48, 1367.
Klang, M. & Murray, A. (Eds.) (2005). Human rights in the digital age. London: Cavendish.
Lessig, L. (2001). The future of ideas. New York: Vintage Books.
Lessig, L. (2006). Code Version 2.0. New York: Basic Books.
Lin, A. C. (2007). Size matters: Regulating nanotechnology. Harvard Environmental Law Review, 31, 349. at 361–374.
MacCormick, D. N. (1977). Rights in legislation. In P. M. S. Hacker & J. Raz (Eds.), Law, morality, and society (p. 189). Oxford: Clarendon.
Mandel, G. N. (2008). Nanotechnology governance. Alabama Law Review, 59, 1.
Manson, N. C., & O’Neill, O. (2007). Rethinking informed consent in bioethics. Cambridge: Cambridge University Press.
Marchant, G. E., & Sylvester, D. J. (2006). Transnational models for regulation of nanotechnology. Journal of Law, Medicine and Ethics, 34, 714–725.
McHale, J. V. (2008). Nanomedicine—small particles, big issues: A new regulatory dawn for health care law and bioethics? In M. Freeman (Ed.), Law and bioethics (p. 376). Oxford: Oxford University Press.
Moor, J. H. (2008). Why we need better ethics for emerging technologies. In J. van den Hoven & J. Weckert (Eds.), Information technology and moral philosophy (pp. 26–39). Cambridge: Cambridge University Press.
NCB. (1999). Genetically modified crops: The ethical and social issues (p. 162). London: Nuffield Council on Bioethics.
Noah, L. (2000). Rewarding regulatory compliance: The pursuit of symmetry in products liability. Georgetown Law Journal, 88, 2147.
O’Neill, O. (2003). Some limits of informed consent. Journal of Medical Ethics, 29, 6.
Phelps, T. A. (2007). The European approach to nanoregulation. In M. Nigel, S. de Cameron & M. E. Mitchell (Eds.), Nanoscale (p. 189). Hoboken, NJ: Wiley.
RCEP. (2008). Novel materials in the environment: The case of nanotechnology. London: Royal Commission on Environmental Protection.
Reidenberg, J. R. (1998). Lex Informatica: The formulation of information policy rules through technology. Texas Law Review, 76, 553.
Reidenberg, J. R. (2005). Technology and Internet jurisdiction. University of Pennsylvania Law Review, 153, 1951.
Sandel, M. (2007). The case against perfection. Cambridge, MA: Harvard University Press.
Sandler, R., & Kay, W. D. (2006). The national nanotechnology initiative and the social good. Journal of Law Medicine, and Ethics, 34, 675.
Spinello, R. A. (2006). Cyberethics: Morality and law in cyberspace (3rd ed.). Sudbury, MA: Jones and Bartlett.
Stewart, R. B. (2002). Environmental regulatory decision making under uncertainty. In T. Swanson (Ed.), An introduction to the law and economics of environmental policy: Issues in institutional design (p. 71). Amsterdam: Elsevier.
Sunstein, C. (2005). Laws of fear. Cambridge: Cambridge University Press.
ten Have, H. (2006). UNESCO and Ethics of Science and Technology. In UNESCO (Ed.), Ethics of science and technology: Explorations of the frontiers of science and ethics, 5–16, at 6. Paris: UNESCO.
van Calster, G., & Bowman, D. (2008). Sufficient or deficient? A review of the adequacy of current EU legislative instruments for regulating nanotechnologies across three industry sectors. Presented at the TILT “Tilting Perspectives on Regulating Technologies” conference, University of Tilburg, December 10 and 11, 2008 (on file with author).
van den Daele, W. (2007). Legal framework and political strategy in dealing with the risks of new technology: The two faces of the precautionary principle. In H. Somsen (Ed.), The regulatory challenge of biotechnology (p. 118). Cheltenham: Elgar.
van den Hoven, J. (2007). Nanotechnology and privacy: Instructive case of RFID. In F. Allhoff, P. Lin, J. Moor & J. Weckert (Eds.), Nanoethics (p. 253). Hoboken, NJ: Wiley.
Wardak, A., & Gorman, M. E. (2006). Using trading zones and life cycle analysis to understand nanotechnology regulation. Journal of Law, Medicine and Ethics, 34, 695.
Weckert, J., & Moor, J. (2007). The precautionary principle in nanotechnology. In F. Allhoff, P. Lin, J. Moor & J. Weckert (Eds.), Nanoethics, Ch. 10. Hoboken, NJ: Wiley.
Wilson, R. F. (2006). Nanotechnology: The challenge of regulating known unknowns. Journal of Law, Medicine and Ethics, 34, 704–713.
Yusuf, A. A. (2007). UNESCO standard-setting activities on bioethics: Speak softly and carry a big stick. In F. Francioni (Ed.), Biotechnologies and international human rights (p. 85). Oxford: Hart.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Brownsword, R. Nanoethics: Old Wine, New Bottles?. J Consum Policy 32, 355–379 (2009). https://doi.org/10.1007/s10603-009-9100-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10603-009-9100-2