The
United States Department of Agriculture (USDA), the Food and Drug Administration (FDA), and the Environmental Protection
Agency (EPA), along with state governments, regulate genetically modified
organisms (GMOs) and are responsible for letting the public which GMO products
are safe (Curtis, 2005). GMOs are used
to create plants that are drought resistant, pest resistant, or ripen on the vine
while shipping. There are no regulations
requiring companies to mark the labels of GMO plants or animals fed GMO feed.
However, there
is a process that must be followed to grow GMO crops. Companies that wish to produce or grow a GMO
crop must first obtain a permit from the USDA (Curtis, 2005). Common crops, like corn or wheat, can be
field tested while the company is under the notification procedure; however,
plants used for pharmacology must wait for the permit (Curtis, 2005). The main factor for the USDA or the FDA is
the safety of the food product and not necessarily that it was produced in a new
way.
There
is a different process for GMOs in Europe, however. The European Commission requires labeling on
products containing more than 0.9% GMO (Habeck, 2003). The industry must also keep records of
products that either contain GMOs or are produced by GMOs (Habeck, 2003). The European Commission’s labeling of GMO
products gives consumers informed consent.
The EU’s regulatory process for GMOs
is a longer process than that of the United States. Because the European Commission regulates
both the product and the process, the regulatory process can take up to 2-3
times longer than in the United States (Kelch et al, 1998). This process was put in place because the EU
could not determine the long-term effects of GMOs (Kelch et al, 1998).
These
regulations, coupled with the United States inability to measure the amounts of
GMO in a product, have led to the European Union banning shipments of United
States corn gluten animal feed because there is no effective way to test for
Bt10 (Casert, 2005). The process that
the European Commission uses takes too long for the United States crops to be
able to be imported. This has resulted
in about a $450 million loss in corn gluten feed for the United States in one
year (Casert, 2005).
In
1997, United States representatives met with European Union scientists and
regulators to discuss the new GMO regulations.
The purpose of this meeting was to find out the details of the new
labeling regulations for GMOs and determine its effect on trade from the United
States with countries in the European Union (Reuter, 1997). The United States representatives were also
interested in whether the European Union was going to discipline member
countries that went their own way with GMOs
(Reuter, 1997).
On
August 18, 2003, the United States joined Argentina and Canada in requesting
the World Trade Organization (WTO) settle the dispute between them and the EU
over the GMO ban (HKTDC, 2003). The
United States is using testimony from scientists showing the safety of GMOs
(IPT, 2003). The United States Trade
Representative and the United States Secretary of Agriculture argue that the
actions of the European Union are hurting biotechnology and the bottom line for
the farmers (IPT, 2003).
It
is the position of the USDA that GMOs should not need to be labeled as such if
there is no significant difference in the nutritional content of the product
(Kelch et al, 1998). Consumer perception
is also a factor. It is possible that
consumers would consider a product labeled as GMO negatively even though
scientists have approved it. Also, the
USDA believes that because of the “coordinated framework” in place, GMOs are
safe and monitored; therefore, adding a label is unnecessary (Kelch et al,
1998).
The
WTO has requested the Dispute Settlement Body to set up a panel to help settle
the case. There are several factors that
complicate the case. First, there is no
definitive way to measure the amount of GMO in a product. Second, the USDA and the EU have different
approaches to regulating GMOs. Third,
not all member states of the EU are in compliance with the European Union
regulations; for example, France does not allow GMOs (Reuter, 1997). With these factors and the differences in
regulating the process of GMOs as well as the product, the WTO may still be
years from resolution.
Casert,
Raf (2005) EU to ban suspected GMO corn
imports. Retrieved on June 25, 2012,
from http://www.usatoday.com/tech/news/biotech/2005-04-15-eu-bans-gluten-imports_x.htm
Curtis,
Patricia (2005) Guide to Food Laws and Regulations
Blackwell Publishing
Habeck,
Martina (2003) Europe’s new rules on
GMOs. Frontiers in Ecology and the Environment, 1(8), 400. Ecological Society of America
HKDTC
(2003) EU’s GMO stance angers US and
others, leads to WTO action. Retrieved
on June 25, 2012, from http://info.hktdc.com/alert/eu0318b.htmI
Kelch,
David; Simone, Mark; Madell, Mary Lisa (1998)
Biotechnology in Agriculture Confronts Agreements in the WTO. Retrieved on June 26, 2012, from www.ers.usda.gov/publications/wrs984/wrs984e.pdf
IPT
(2003) USDA takes EU to WTO over
GMO. Retrieved on June 26, 2012, from http://www.iptv.org/mtom/story.cfm/lead/7357/mtom_20030516_2836_lead2
Reuter
(1997) USDA Pressures EU officials over
GMO foods. Retrieved on June 26, 2012,
from http://www.gene.ch/gentech/1997/8.96-5.97/msg00210.html
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