Counterparts Agreement Vertaling

Since then, the proposals have been thoroughly reviewed by the Council and the European Parliament and these two institutions reached agreement on the final texts in July 2003. Overall, the final texts retain the main features of the Commission`s initial proposals. The new regulations are expected to be published in the Official Journal in the fall of this year and will come into effect shortly thereafter. The UNEP Cartagena Biosecurity Protocol of the Convention on Biological Diversity was adopted on 29 January 2000. The overall aim of this UN convention is to set common rules for cross-border GMO movements to ensure the protection of biodiversity and human health around the world. 11. Maize MON 863 X MON 810 (protection against certain pests) Other rules on cultivation conditions and other purity requirements for the presence of genetically modified seeds in traditional seed lots, as well as detailed labelling rules, should be adopted. The current regulation does not include any new specific EU provisions for imports or GMO movements between Member States. These measures will continue to be covered by existing EU legislation. Eight applications for genetically modified foods are currently underway at various stages of the licensing process, including genetically modified maize products, sugar strokes and soybeans. (see Appendix 3).

If this is not the case, the draft decision is submitted to the Council of Ministers by qualified majority or rejection. If the Council does not rule within three months, the Commission can adopt the decision. In response to the BSE crisis, legislation has been introduced for a specific traceability system for beef products (Regulation 1760/2000/EC). The Council and Parliament Regulation (EC/178/2002 Regulation), which sets out the general principles and general requirements of food legislation, also establishes the principle of traceability at all stages of the production and distribution chain in the food and feed sector. What is the procedure for authorizing the release of GMOs into the environment? On 25 July 2001, the European Commission adopted two legislative proposals on GMOs. These proposals were closely linked and sewed at the same time; How does the environmental impact assessment procedure work from October 17, 2002? Information about the supplier, customer, price and date of transaction, as well as the nature, source, content and quantity of the product, already accompany most transactions. Directive 2001/18 contains general provisions on which a GMO traceability system could be based, but not a definition of GMO traceability, neither traceability targets nor a comprehensive approach to their implementation. The transposition of the Cartagena Protocol on the Prevention of Biotech Risks into EU legislation is based on a wide range of biotechnology legislation applicable to the use of GMOs in the European Union, including imports. The 2001/18/EC Directive on the Voluntary Release of Genetically Modified Organisms into the Environment is at the heart of this legislative framework. . The marketing authorization for medicines for human and veterinary use (including those obtained from genetically modified organisms) is governed by Regulation (EEC) 2309/93, which provides for Community procedures for the authorisation and monitoring of medicines for human and veterinary use.

9. Rape, which is tolerant to glufosinate ammonium (C/DE/98/6) from Germany (C/DE/98/6), has been received by the Commission 90/220: 29.10.98 Clear rules are already established in the EU for the assessment and authorisation of GMOs and genetically modified foods, but the powers are currently shared between the Member States and the Community.

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