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Put Down the Genetically Modified Tomatoes -- It's no time to pick a trade fight over biotech foods.
Dr.
Stuart S.
Malawer
Legal Times
(09-01-2003)
Food
fights are in poor taste among fraternity brothers or infant siblings. Among
trading nations, they make even less sense. Before an unnecessary dispute over
genetically modified foods spirals out of control, the United States should
drop a World Trade Organization action recently initiated against the European
Union.
Instead, the United States should negotiate its trade concerns
in a diplomatic setting. Friendly transatlantic relations are more important
now than ever before. Besides, the United States will probably lose this case.
The point of contention is this: Since 1998, the EU has
observed a de facto moratorium on approvals to import biotech products —
basically, agricultural and foodstuffs. In addition, the United States
contends, several individual European states have banned the marketing and
importation of biotech products (though some products have been approved).
In May, the United States filed a formal complaint with the
WTO over the EU moratorium. A 60-day consultation period followed. In August,
with no resolution in sight, the United States asked the WTO to establish a
dispute settlement panel.
SAFETY STANDARDS
The United States argues that three EU actions violate WTO
law: the suspension of consideration of applications and granting of approvals
for biotech imports; the failure to consider specific enumerated products; and
the individual national bans on marketing and importation of biotech products.
The United States relies on the Sanitary and Phytosanitary
Agreement, one of the Uruguay Round of Multilateral Agreements. Article 2
provides that WTO members can take measures to protect human life or health,
provided they have a basis in scientific principles and do not arbitrarily
discriminate between members. Article 3 requires such measures to be based upon
international standards, where those standards exist. It specifically cites the
Codex Alimentarius Commission as an international organization responsible for
developing acceptable standards. Article 5(1) requires a risk assessment that
takes into account techniques developed by relevant international
organizations. Article 5(7) provides that when the scientific evidence is
insufficient, members may apply restrictive measures provisionally.
The United States also argues that the EU moratorium is
inconsistent with the Uruguay Round's Technical Barriers to Trade Agreement,
which mainly concerns product labeling. Article 2(2) requires that technical
regulations not create unnecessary obstacles to trade. Article 2(4) provides
that states base such regulations on relevant international standards.
This legal structure governing the international food trade
came into existence in 1995 along with the WTO. What makes it unusual is that international
standards developed outside the WTO framework are explicitly
incorporated into the WTO system to determine the legality of members' actions.
Before the explosion of biotech research over the last decade — and before
consumers and governments worldwide became apprehensive about genetically
modified foods — there was little understanding of how these standards might
affect international trade.
The incorporation of the Codex Commission into the Sanitary
and Phytosanitary Agreement thrust an obscure body into the center of global
trade disputes. The Rome-based commission was created in 1963 by two
specialized United Nations agencies, the Food and Agricultural Organization and
the World Health Organization. Before 1995, its standards were mainly voluntary
food safety measures that states might take into account.
Now the Codex standards have become benchmarks against which
national trade measures concerning food imports and labeling are assessed for
compliance with WTO obligations. A national law unsupported by these standards
may be deemed an illegal trade barrier.
Thus, the U.S. case against the EU depends primarily on
whether regulations adopted by the EU are consistent with standards promulgated
by the Codex Commission. Can the United States persuade a WTO panel that the
EU's risk assessments did not conform with Codex standards and, thus, that
there is no scientific evidence to support the measures of the EU or its member
states — and that where the EU relies on the precautionary principle, there was
scientific evidence that it overlooked?
A WEAKER CASE
Codex Commission actions since May have produced serious
problems for the U.S. case. Recent actions by the European Parliament raise
additional questions. The EU's July suit against 11 member states in the
European Court of Justice makes significant complications for the U.S.
proceedings in the WTO. Perhaps more importantly, issues of foreign policy and
national security — namely, the U.S. desire to rebuild transatlantic ties in
light of the war on terrorism and peace efforts in the Middle East and Iraq —
call into question the wisdom of continuing this fight.
The United States argues that it simply wants the EU to apply
a scientific, rules-based process to the review and approval of genetically
modified food imports developed through agricultural biotechnology. The EU
contends that a new regulatory framework that entered into force in 2002 does
just that.
This summer, the European Parliament also approved legislation
setting strict labeling and tracing requirements for food or feed made with
genetically altered organisms. These laws are expected to receive final EU
approval in the fall, prior to any WTO panel decision. They would permit
genetically modified foods to be imported if they comply with the new
requirements — which would, very likely, render the U.S. action moot.
Further clouding matters is the Codex Commission's recent
adoption of the first international guidelines for risk assessment studies of
genetically modified foods. The guidelines require safety evaluations before
food products are placed on the market. They also require that food products be
traceable back to their origins. The U.S. Food and Drug Administration, by
contrast, does not require a premarket safety assessment or an assessment of
unintended consequences due to gene modification.
All these emerging standards appear to support stronger, not
weaker, regulation of genetically modified foods. Thus, the EU's position seems
more justifiable today than yesterday: It is relying on scientific evidence or,
where there is not enough, it is taking precautions while seeking more
information.
In July, the EU brought suit in the European Court of Justice
against 11 member states contending that they (and implicitly not the EU) are
maintaining illegal moratoriums against biotech foods. Although international
law imposes liability on a country when a political subdivision violates an
international obligation, this rule does not apply to the EU. It is merely a
regional grouping, not liable for its members' actions. Thus the Court of
Justice filing foreshadows a strong defense in any WTO action concerning EU
responsibility for its members' biotech moratoriums.
ABUSE OF PROCESS
Add up the evidence, and it seems that the U.S. case is more
about politics than science. It responds to the special pleas of agricultural
firms, and it has been brought in anger (and as part of a defensive legal
strategy) over recent U.S. losses in the WTO on other trade issues —
anti-dumping duties, export tax subsidies, and steel tariffs. It evidences a
growing U.S. tendency to rely upon power politics and unilateral intimidation
at the expense of diplomatic and multilateral efforts.
But this approach is shortsighted. If there is anything truly
multilateral in the world, it is trade relations. The United States was the
primary architect of the WTO's dispute resolution system and is a most
aggressive user today. Within the last few weeks alone, the United States has
prevailed in actions brought by India (rules of origin and textile imports), by
Japan (sunset review of anti-dumping duties), and against Japan (testing of
agricultural imports). It is in the U.S. national interest not to abuse this
system.
Litigation, especially in a losing case designed to appease
unwarranted congressional angst, is not good public policy. While U.S.
agricultural firms may have real grievances, they should not be settled by a
WTO suit — at least not now. Negotiating labeling requirements with the EU
makes a lot more sense: Agree to disclose the information, and let the buyer
and market decide.
The United States must beware that litigation is never viewed
as a friendly act. And these days the United States needs friends to face much
graver problems of terrorism and peace. We need to make the world a safer place
not for genetically modified organisms, but for all of us. In short, drop this
food fight now and get on with building a safer international community.
Stuart S. Malawer is the Distinguished Service Professor of
Law & International Trade at George Mason University's School of Public
Policy. He can be reached at stuartmalawer@msn.com.