Which programmes/actions
are being developed at international level?
International initiatives have been established under the short-
and medium-term actions of the Commission's strategy. The Commission
recognised that owing to the resources required to achieve its proposed
actions (in terms of scientific expertise, cost etc), international
cooperation was imperative. International co-operation affords the
following benefits:
- Prevents duplication of research, testing and assessment.
- Enables the development of internationally recognised test systems
and strategies.
- Spreads the financial cost and speeds up the process of testing
and assessment.
- Allows access to different expertise.
The programmes and actions being developed at international level
are listed below:
International information exchange and co-ordination
Under the short-term actions of the Commission's strategy, the exchange
of information and international co-ordination is essential to remain
abreast of research results and avoid duplication, as well as ensuring
that international trade agreements are not infringed when considering
policy actions. The following international collaborations have been
set up to achieve these goals:
- EU/WHO/IPCS: Co-ordination of international research and development
through the formation of the Global Endocrine Disruption Research
Inventory
- WHO/IPCS: Global assessment of the state-of-the-science of endocrine disruptors - an assessment prepared by an expert group on behalf of the World
Health Organization, the International Labour Organisation, and
the United Nations Environment Programme.
- EU-US Science and Technology Agreement: Under this agreement,
a joint meeting was held in Italy in 1999. Common research priorities
were identified and, subsequently, funding for research was made
available by the Commission and the US Environmental Protection
Agency (US EPA).
In 2003 the Commission
finalised a study on "Information
Exchange and International Coordination on Endocrine Disruptors" carried out by MRC Institute for Environment
and Health (UK), with the aim to assess the global initiatives
on Endocrine Disruptors, concerning regulatory, testing and research
activities and make recommendations on ways to improve coordination
and the sharing of the workload.
The study comprised a number of interrelated elements. Information on
activities, opinions, approaches and outputs of various countries
and stakeholder organisations was obtained through interviews, supplemented
with data from websites. The information obtained was subject to detailed
critical analysis to compare and contrast the approach of the EC with
those of its Member States and the governments of the USA and Japan.
In addition, key reports and assessments published by governmental
organisations or other authoritative bodies
were identified, and short summaries prepared to further highlight
relevant findings, opinions, decisions and recommendations.
Complete final report and
annexes:
-
Executive
Summary
-
MRC
report
-
Annex 1 Summary table of interview findings
-
Annex
2a Interview transcripts - EU Member States
-
Annex
2b Interview transcripts
- Non European countries
-
Annex
2c Interview transcripts
- Non governmental organisations
-
Annex
3 Some websites of
EU Member States not interviewed
-
Annex
4a Summaries of key
reports, assessments and other documentation - National responses,
strategies and legislation
-
Annex
4b Summaries of key
reports, assessments and other documentation - Research and
development, and monitoring
-
Annex
4c Summaries of key
reports, assessments and other documentation -Testing,
screening and prioritisation
-
Annex
4d Summaries of key
reports, assessments and other documentation - Current concerns
-
Annex
4e Summaries of key
reports, assessments and other documentation -Miscellaneous
-
Annex
4f Summaries of key
reports, assessments and other documentation - Full bibliography
(pdf ~4M)
International development and validation of tests
and test strategies
- EU/OECD/US : The Commission participates in the Endocrine disruptors
testing and assessment task force (EDTA), which was set up to collaborate
with other national and international bodies to achieve co-operation
in developing and validating new tests and test strategies that
are complimentary and will be recognised and accepted by different
international and national organisations.
- EU-US Science and Technology Agreement: Under this agreement the
Commission and the US EPA have agreed to share information on priority-setting
of chemicals, screening and testing development and validation and
research activities.
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