Progress: Awaiting committee decision
Role | Committee | Rapporteur | Shadows |
---|---|---|---|
Lead | ENVI | TSIODRAS Dimitris ( PPE) | CLERGEAU Christophe ( S&D) |
Former Responsible Committee | ENVI | SPYRAKI Maria ( EPP) | |
Committee Opinion | BUDG | ||
Committee Opinion | ITRE | ||
Committee Opinion | AGRI | ||
Former Committee Opinion | BUDG | VAN OVERTVELDT Johan ( ECR) | |
Former Committee Opinion | ITRE | ||
Former Committee Opinion | AGRI | LINS Norbert ( EPP) |
Lead committee dossier:
Legal Basis:
TFEU 043, TFEU 114, TFEU 168-p4, TFEU 192-p1, TFEU 207
Legal Basis:
TFEU 043, TFEU 114, TFEU 168-p4, TFEU 192-p1, TFEU 207Subjects
Events
PURPOSE: to amend Regulations (EC) No 178/2002, (EC) No 401/2009, (EU) 2017/745 and (EU) 2019/1021 of the European Parliament and of the Council as regards the re-attribution of scientific and technical tasks and improving cooperation among Union agencies in the area of chemicals.
PROPOSED ACT: Regulation of the European Parliament and of the Council.
ROLE OF THE EUROPEAN PARLIAMENT: the European Parliament decides in accordance with the ordinary legislative procedure and on an equal footing with the Council.
BACKGROUND: the Commission has, in its Communication ‘European Green Deal’, set an objective that chemical safety assessments should move towards a process of ‘one-substance, one-assessment’, calling for more transparent and simpler risk assessment processes in order to reduce the burden on all stakeholders, accelerate decision-making, as well as to increase consistency and predictability of scientific decisions and opinions.
To achieve that objective, part of the scientific and technical work on chemicals performed at Union level in support of Union legislation needs to be reattributed to the most suitable Union agencies. This would simplify the current set-up, improve quality and coherence of safety assessments across Union legislation, and ensure more efficient use of existing resources.
CONTENT: this proposal proposes targeted amendments to attribute tasks in Regulation (EU) 2019/1021 on persistent organic pollutants, and Regulation (EU) 2017/745 on medical devices. The proposal also amends Regulation (EC) No 401/2009 establishing the European Environmental Agency and Regulation (EC) No 178/2002 laying down the general principles and requirements of food law and establishing the European Food Safety Authority. These amendments will ensure good cooperation among EU agencies on all aspects involving the consistency and efficiency of chemical assessments. These include the development of methodologies, data exchanges and reconciling divergence in scientific output.
The proposal:
- amends Regulation (EC) No 178/2002 (General Food Law Regulation). It includes provisions enabling EFSA to better cooperate and coordinate with ECHA, EMA and EEA . This cooperation would lead to more consistent scientific assessments of chemicals and encourage the agencies to develop consistent scientific opinions and methodologies, taking into account specific sectoral characteristics. The provisions on data and information exchange would bring the EU a step closer to the one substance, one assessment goals. These provisions make greater interoperability possible and scientific processes more robust;
- amends Regulation (EC) No 401/2009 (the EEA Founding Regulation). It includes streamlining obligations on the EEA to promote and coordinate the development of assessment methodologies and places cooperation obligations on the EEA;
- amends Annex I of Regulation (EU) 2017/745 (the Medical Devices Regulation) to task ECHA with updating existing guidelines on conducting the risk-benefit assessment of the presence of phthalates in medical devices. The agency will also develop guidelines for other substances, which are classified as either carcinogenic, mutagenic or toxic to reproduction, of category 1A or 1B or have endocrine disrupting properties for human health of Category 1;
- amends Regulation (EU) No 2019/1021 by giving the Commission the possibility to request ECHA to develop a report analysing the human health, environmental, social, and economic impact of introducing or modifying concentration limit values specified in Annexes IV and V to Regulation (EU) No 2019/1021 (POPs Regulation).
Considering the highly technical nature of the amendments, this provision also introduces the adoption of amendments to Annexes IV and V by means of a delegated act. To promote the development of a comprehensive chemical exposure and toxicity knowledge base, as well as streamline data flows in line with the one substance, one assessment policy target, the provision also diverts data flows on the presence of persistent organic pollutant substances in the environment to EEA, which is the agency responsible for collecting occurrence data on chemicals in the environment.
Documents
- Contribution: COM(2023)0783
- Contribution: COM(2023)0783
- Economic and Social Committee: opinion, report: CES5710/2023
- Document attached to the procedure: EUR-Lex
- Document attached to the procedure: SWD(2023)0850
- Legislative proposal published: COM(2023)0783
- Legislative proposal published: EUR-Lex
- Document attached to the procedure: EUR-Lex SWD(2023)0850
- Economic and Social Committee: opinion, report: CES5710/2023
- Contribution: COM(2023)0783
- Contribution: COM(2023)0783
History
(these mark the time of scraping, not the official date of the change)
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