Regulation on the market of products containing, consisting of or produced from genetically modified cotton COT102, pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council
This resolution expresses the European Parliament's objection to a Commission decision that would allow genetically modified cotton COT102 to be placed on the market for food and feed. The decision affects consumers, animal feed producers, and potentially the environment, as the cotton contains genes for insecticidal proteins and antibiotic resistance. Concerns include the potential for increased toxicity of insecticidal proteins, unknown effects on non-target organisms, and the use of antibiotic resistance genes, which is discouraged by EU law. The Parliament calls for the Commission to repeal the decision, citing a lack of qualified majority support from Member States and previous objections to similar products.
Analysis
The European Parliament resolution concerns Commission Implementing Decision (EU) 2024/2627, which authorizes the placing on the market of products containing, consisting of, or produced from genetically modified cotton COT102.
What changes
- The European Parliament calls on the Commission to repeal Implementing Decision (EU) 2024/2627.
- The European Parliament calls on the Commission to submit a new draft decision to the committee.
- The European Parliament reiterates its call on the Commission not to authorize the placing on the market of any GM plants containing genes which confer antimicrobial resistance.
Expected impact
- The resolution considers that Implementing Decision (EU) 2024/2627 exceeds the implementing powers provided for in Regulation (EC) No 1829/2003.
- The resolution considers that Implementing Decision (EU) 2024/2627 is not consistent with Union law, specifically not compatible with the aim of Regulation (EC) No 1829/2003 to ensure a high level of protection for human life and health, animal health and welfare, and environmental and consumer interests, while ensuring the effective functioning of the internal market.
- Authorizing GM plants containing genes conferring antimicrobial resistance would be in violation of Article 4(2) of Directive 2001/18/EC, which calls for a phase-out of antibiotic resistance marker genes (ARMGs) that may have adverse effects on human health or the environment.
Limitations
- The document is a resolution from the European Parliament and does not contain the full text of the Commission Implementing Decision (EU) 2024/2627 or the EFSA scientific opinion, limiting the ability to analyze the specific technical details of the authorization itself.
- The document does not provide detailed information on the specific uses of cottonseed oil and flour beyond general examples, which limits a comprehensive analysis of potential human exposure pathways.
- The document does not include the full list of Member States' critical comments submitted to EFSA, only summarizing the nature of these comments.
- The document does not detail the specific 'adverse effects' on non-target organisms or the 'out-of-range' species mentioned in the context of Bt toxins, beyond referencing peer-reviewed publications.
- The document does not provide the full text of the Commission's letter of September 11, 2020, regarding the need to take sustainability into account for GMO authorization decisions.
Shadow Rapporteurs
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