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ICTSD Outputs and Activities on Biotechnology, Trade and Sustainble DevelopmentBiotechnology Home
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| WTO Dispute Biotechnology: Addressing Key Trade and Sustainability IssuesB.2 Multilateral trade rulesQ14 What is the role of international standard-setting bodies?The harmonisation of measures and regulations based on international
standards is one of the primary objectives of both the SPS and TBT
agreements. Indeed, sanitary and phytosanitary measures and technical
regulations based on international standards are presumed to be
consistent with WTO rules. As a result, the standards and guidelines
developed by international standard-setting bodies in the field
of biotechnology will be critical in determining the measures and
regulations that may be adopted by WTO Members in relation to genetically
modified organisms and products. The SPS Agreement establishes that sanitary or phytosanitary measures
that conform to international standards, guidelines or recommendations
of the following international standard-setting bodies are presumed
to be consistent with its provisions: (1) the Codex Alimentarius
Commission (Codex) in relation to food safety; (2) the World Organization
for Animal Health (OIE); (3) the Secretariat of the International
Plant Protection Convention for plant health; and (4) other relevant
international organisations open for membership to all Members,
as identified by the SPS Committee, for matters not covered by the
previous organisations, though no additional body has thus far been
agreed upon. Of these international standard-setting bodies, both
the Codex and the International Plant Protection Convention (IPPC)
have already developed biotechnology-related standards and guidelines
(see also C.6 and C.7). An Ad Hoc Intergovernmental Task Force on Foods Derived from Biotechnology
was created by the Codex to develop standards, guidelines or recommendations,
as appropriate, for foods derived from biotechnology or traits introduced
into foods by biotechnology. These standards, guidelines, and recommendations
are to be developed on the basis of scientific evidence, risk analysis
and having regard, where appropriate, to other legitimate factors
relevant to the health of consumers and the promotion of fair trade
practices. To date, the Codex has adopted three standards relevant
to biotechnology, including the Principles for the Risk Assessment
of Foods Derived from Modern Biotechnology and the Guidelines
for the Conduct of Food Safety Assessment of Foods Derived from
Recombinant-DNA Plants. Efforts are also under way in the
Codex towards developing labelling standards for biotechnology foods. At the IPPC, the 2001 report of a working group on the phytosanitary
aspects of genetically modified organisms and biosafety recommended
as a matter of urgency that detailed standard specifications
be drafted, in co-ordination with CBD experts, in the biotechnology
context. A standard for the Pest risk analysis for quarantine
pests including analysis of environmental risks and living modified
organisms, for example, was adopted in 2004. In 2005, the OIE adopted several resolutions on genetically engineered
animals and the relationship between the implementation of the organisations
standards and international trade. OIE members stressed the importance
of developing standards in this field. Although genetically engineered
animals are subject to the organisations overall risk assessment
standards, some members raised concerns about the unique risks posed
by this type of engineering and the lack of standards for regulations
that aim to address them. OIE members thus created an Ad Hoc Group
on Biotechnology and asked the Secretariat to develop and adopt
standards and guidelines for: research and use of vaccines for animals
produced through biotechnology, animal health risks linked to cloning,
exclusion of unapproved animals and products from the livestock
population and segregation from the feed and food supply, and animals
that have been genetically engineered to produce medicines or chemicals
(ICTSD, 2005b). The TBT Agreement, unlike the SPS Agreement, does not limit the sources of international standards that WTO Members may use for their technical regulations for a presumption of not being unnecessarily trade-restrictive. As a result, other international standards on biotechnology become relevant, such as those developed by the International Organization for Standardization (ISO). The ISO is a non-governmental organisation that links the national standards institutes of 156 countries. In the ISO, the technical committee on food products, which addresses standardisation in the field of human and animal foodstuffs as well as animal and vegetable propagation materials, in particular terminology, sampling, methods of test and analysis, product specifications and requirements for packaging, storage and transportation, has a working group on GMOs and derived products. This technical committee has developed, for instance, standards on the methods of analysis for the detection of GMOs and derived products in foodstuffs. In addition, it has been argued that the provisions of the Cartagena
Protocol on Biosafety, as well as the work conducted by the Conference
of the Parties (COP) acting as Meeting of the Parties (MOP) (see
Section B.3), for instance, could play a significant role as international
standards in the context of the TBT Agreement. For example, Article
18 of the Biosafety Protocol provides for handling, transport, packaging
and identification of living modified organisms that are subject
to intentional transboundary movement and requires the COP-MOP to
consider the need for and modalities of developing standards with
regard to identification, handling, packaging, and transport practices.
It is interesting to note that the Conference of the Parties serving
as the meeting of the Parties to the Biosafety Protocol included
a specific request to the Executive Secretary to establish co-operation
with the World Customs Organization, the ISO, the United Nations
Transport of Dangerous Goods Sub-Committee, the International Air
Transport Association and other relevant customs and transport organisations,
with a view to developing harmonised approach for the packaging
and transport of living modified organisms (and the Secretariat
eventually included the Codex in its consultations), highlighting
the difficulties raised by the fragmentation of standards related
to biotechnology. |
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© ICTSD 2004 - Last Update:
23-Jul-2007
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