Nanotech Under the Microscope
(Page 2 of 2)
July / August 2004
Anne Geske Utne magazine
According to Jim Thomas in The Ecologist (Feb.
2004), the Food and Drug Administration and other agencies are
'privately admitting they have made a mistake in letting
nanoproducts onto the market without safety studies, and are
looking for ways to tweak existing regulations.' Thomas, whose
Nanowatch column appears in the London-based magazine, is the
European program manager for the Action Group on Erosion,
Technology and Concentration, or ETC Group. A 2003 communiqu?
posted by the Winnipeg-based ETC Group (www .etcgroup.org)
highlights the central problem with the current push to
commercialize nanotech. Many companies have dismissed the idea that
particles approved for commercial use at much larger sizes ought to
be retested in their nano form, the watchdog group notes. That's
ironic, given that 'the impetus for their development stemmed from
the radical changes that can happen when a substance is reduced to
the nano scale.'
RELATED CONTENT
Although billions of U.S. federal dollars are now slated for
nanotech research and development, only about 11 percent of that
money is earmarked this year for health and environmental studies.
Some of the studies will take years to complete; others could yield
results more quickly. While the call for more research is spreading
along with concern, there are currently no specific regulations to
control the release of products containing nanoparticles in any
country -- and no labeling requirements either. With the widespread
use of nanotechnology now looming in agriculture, medicine, and
other crucial fields, critics call it another example of an
industry moving ahead without fully investigating potential
long-term consequences.
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