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Date: 2021-03-09 Category: Not Applicable State: Union Government Country: Europe

Commission Implementing Regulation (EU) 2021/412 of 8 March 2021 amending Implementing Regulation (EU) 2017/962 as regards the review of the suspension of the authorisation of ethoxyquin as a feed additive (Text with EEA relevance)

Issued by European Commission · Directorate-General for Health and Food Safety

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Executive Summary & Key Takeaways

Executive Summary: This regulation amends Implementing Regulation (EU) 2017/962, postponing the review of the suspension of ethoxyquin as a feed additive. The review is now due by December 31, 2022, at the latest, or after a non-favourable opinion from the European Food Safety Authority (EFSA) on the safety and efficacy of ethoxyquin. This extension is necessary to allow EFSA sufficient time to complete its assessment of supplementary data submitted by the applicant. Key Points / Main Content: * **Amendment of Implementing Regulation (EU) 2017/962:** * Article 5 of Implementing Regulation (EU) 2017/962 is replaced. * **Review Deadline Extension:** * The review of the suspension of ethoxyquin is postponed until December 31, 2022, at the latest. * The review will also occur if EFSA adopts a non-favourable opinion on ethoxyquin's safety or efficacy before this date. * **Entry into Force:** * This Regulation enters into force on the third day following its publication in the Official Journal of the European Union. Impact Analysis: **European Food Safety Authority (EFSA):** * *Impact:* EFSA is granted additional time to assess supplementary data related to ethoxyquin's safety and efficacy. * *Action Required:* Complete the assessment of all supplementary information and data submitted or to be submitted by the applicant and provide an opinion. **Applicant (Ethoxyquin Manufacturer):** * *Impact:* The applicant must continue to provide any further information and data requested by EFSA. * *Action Required:* Submit any additional data required by EFSA for the assessment of ethoxyquin's safety and efficacy. **European Commission:** * *Impact:* The Commission must review the suspension measure again by December 31, 2022, or following a non-favourable opinion from EFSA. * *Action Required:* Monitor the EFSA assessment and prepare for a review of the suspension measure by the new deadline. **Member States:** * *Impact:* The regulation is binding and directly applicable in all Member States. * *Action Required:* Implement the regulation.

Key Entities Referenced

European Union: A political and economic union of member states located primarily in Europe. European Commission: An institution of the European Union, responsible for proposing legislation, implementing decisions, upholding the EU treaties and managing the day-to-day business of the EU. Regulation (EC) No 1831/2003: Regulation of the European Parliament and of the Council on additives for use in animal nutrition. European Parliament: The parliamentary assembly of the European Union that, with the Council of the European Union, exercises the legislative function of the EU. Council of the European Union: One of two legislative bodies of the European Union (the other being the European Parliament) and one of its seven institutions. Commission Implementing Regulation (EU) 2017/962: Commission Implementing Regulation suspending the authorisation of ethoxyquin as a feed additive. European Food Safety Authority: The European Union agency that provides independent scientific advice on risks related to food and feed safety. Ursula VON DER LEYEN: President of the European Commission.
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L 81/30 E N O f f i c i a l J o u r n a l o f t h e E u r o p e a n Union 9.3.2021 COMMISSION IMPLEMENTING REGULATION (EU) 2021/412 of 8 March 2021 amending Implementing Regulation (EU) 2017/962 as regards the review of the suspension of the authorisation of ethoxyquin as a feed additive (Text with EEA relevance) THE EUROPEAN COMMISSION, Having regard to the Treaty on the Functioning of the European Union, Having regard to Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition(1), and in particular Article 13(2) thereof, Whereas: (1) Commission Implementing Regulation (EU) 2017/962(2) suspended the authorisation of the additive ethoxyquin on the basis of the opinion of the European Food Safety Authority (‘the Authority’) of 21 October 2015(3), which could not conclude on the safety and efficacy of the additive due to an overall lack of data submitted by the applicant in the framework of the authorisation procedure. (2) The authorisation of the additive ethoxyquin was suspended pending the submission and assessment of supplementary data to be produced by the applicant, in accordance with a time schedule listing in order of priority the studies to be carried out successively. According to that time schedule, the outcome of the last of those studies would be available by July 2018. (3) In accordance with Implementing Regulation (EU) 2017/962, the suspension measure is to be reviewed by 31 December 2020 at the latest, after due assessment of the required supplementary data. (4) While the applicant has submitted successive packages of supplementary data, major delays occurred in the generation of a series of data, in particular concerning the demonstration of the safety of the additive ethoxyquin for the environment. The reasons for those delays include the need to initiate further studies in order to comply with the specific data requirements set out in Commission Regulation (EC) No 429/2008(4) and the related Authority’s detailed guidance, and difficulties in finding appropriate laboratories or testing facilities for the conduction of certain studies. (5) The applicant last submitted supplementary data on the environmental risk assessment in September 2020. Depending on the outcome of the assessment by the Authority of those supplementary data, it cannot be excluded that the applicant may still be requested to provide further information and data. (6) In view of the above, the Authority should be granted sufficient time to complete the assessment process of all supplementary information and data submitted or still to be submitted by the applicant in order to demonstrate the safety and efficacy of the additive ethoxyquin. It is therefore appropriate to postpone the review of the suspension measure until the completion of the assessment process. The new timeframe for the review should be determined in consideration of an estimated maximum period needed for such completion. In any event, the suspension measure should be reviewed where, during the assessment process, the Authority adopts a non-favourable opinion on the safety or efficacy of the additive ethoxyquin. (7) Implementing Regulation (EU) 2017/962 should therefore be amended accordingly. (1) OJ L 268, 18.10.2003, p. 29. (2) Commission Implementing Regulation (EU) 2017/962 of 7 June 2017 suspending the authorisation of ethoxyquin as a feed additive for all animal species and categories (OJ L 145, 8.6.2017, p. 13). (3) EFSA Journal 2015;13(11):4272. (4) Commission Regulation (EC) No 429/2008 of 25 April 2008 on detailed rules for the implementation of Regulation (EC) No 1831/2003 of the European Parliament and of the Council as regards the preparation and the presentation of applications and the assessment and the authorisation of feed additives (OJ L 133, 22.5.2008, p. 1).9.3.2021 E N O f f i c i a l J o u r n a l o f t h e E u r o p e a n Union L 81/31 (8) Taking into account that Implementing Regulation (EU) 2017/962 is to be reviewed by 31 December 2020 at the latest, this Regulation should enter into force as a matter of urgency in order to minimise any legal vacuum. (9) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed, HAS ADOPTED THIS REGULATION: Article 1 Amendment to Implementing Regulation (EU) 2017/962 Article 5 of Implementing Regulation (EU) 2017/962 is replaced by the following: ‘Article 5 Review This Regulation shall be reviewed by 31 December 2022 at the latest and in any event after the adoption by the Authority of a non-favourable opinion on the safety and efficacy of the additive ethoxyquin.’. Article 2 Entry into force This Regulation shall enter into force on the third day following that of its publication in the Official Journal of the European Union. This Regulation shall be binding in its entirety and directly applicable in all Member States. Done at Brussels, 8 March 2021. For the Commission The President Ursula VON DER LEYEN

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