Literature DB >> 19740561

Hitting the mark or falling short with nanotechnology regulation?

Karinne Ludlow1, Diana M Bowman, Dwayne D Kirk.   

Abstract

Regulation of all new technology ebbs and flows between periods of under- and over-regulation, often dependant on the viewpoint of the observer and the underlying objectives of the particular regulation. As illustrated by genetic modification (GM) applications, defining what constitutes appropriate regulation for a rapidly evolving technology can be difficult. Drawing upon the lessons of GM, we argue that nanotechnology will go through similar periods of inappropriate regulation. As with GM, future regulatory responses to nanotechnology will be shaped by perceptions of risk and willingness to accept varying levels of risk. With varying responses between jurisdictions appearing inevitable, we argue that the timing and type of regulation adopted for nanotechnology, and its appropriateness, will be crucial to its commercial success.

Mesh:

Year:  2009        PMID: 19740561     DOI: 10.1016/j.tibtech.2009.07.007

Source DB:  PubMed          Journal:  Trends Biotechnol        ISSN: 0167-7799            Impact factor:   19.536


  2 in total

1.  The problem of regulating sophisticated materials.

Authors:  Andrew Maynard; Diana Bowman; Graeme Hodge
Journal:  Nat Mater       Date:  2011-07-22       Impact factor: 43.841

2.  In vitro genotoxicity testing strategy for nanomaterials and the adaptation of current OECD guidelines.

Authors:  S H Doak; B Manshian; G J S Jenkins; N Singh
Journal:  Mutat Res       Date:  2011-09-28       Impact factor: 2.433

  2 in total

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