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Date: 30-Jan-2025 Category: Not Applicable State: Union Government Country: Europe

Commission Implementing Regulation (EU) 2025/142 of 29 January 2025 concerning the authorisation of a preparation of 6-phytase produced with Trichoderma reesei CBS 126897 as a feed additive for fin fish (holder of authorisation: AB Enzymes Finland Oy)

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

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Executive Summary & Key Takeaways

What it means

  • Commission Implementing Regulation (EU) 2025/142 authorises the use of a preparation of 6-phytase produced with Trichoderma reesei CBS 126897 as a feed additive for fin fish. The additive is classified as a zootechnical additive and a digestibility enhancer. The holder of authorisation is AB Enzymes Finland Oy.

Key Changes

  • Authorisation is granted for 6-phytase produced with Trichoderma reesei CBS 126897 as a feed additive for fin fish.
  • The additive is classified as a zootechnical additive and a digestibility enhancer.
  • The European Food Safety Authority (EFSA) concluded that the preparation is safe for fin fish, consumers, and the environment under the proposed conditions of use.
  • EFSA determined the preparation is a respiratory sensitiser but not a skin or eye irritant or a skin sensitiser.
  • The preparation is considered efficacious for salmonids and ornamental fish at 500 FTU/kg complete feed and for other fin fish at 2500 FTU/kg complete feed.
  • The authorisation is valid until 19 February 2035.
  • Minimum activity of the additive is 5000 FTU/g.
  • Specific direction for use of the additive and premixtures must include storage conditions and stability to heat treatment.
  • Users of the additive and premixtures must establish operational procedures and organisational measures to address potential risks. If risks cannot be eliminated, personal breathing protective equipment must be used.

Impact Analysis

Fish Feed Manufacturers

  • Must comply with the requirement to include storage conditions and stability to heat treatment in the directions for use of the additive and premixtures.

AB Enzymes Finland Oy (Holder of Authorisation)

  • Must provide users with information on storage conditions and stability to heat treatment.

Fish Farmers

  • Must follow the directions for use of the additive and premixtures, including the use of personal breathing protective equipment if risks cannot be eliminated by operational procedures and organisational measures.

Feed Additive Distributors and Premixture Manufacturers

  • Must establish operational procedures and organizational measures to address potential risks resulting from the use of the additive. Where those risks cannot be eliminated, the additive and premixtures shall be used with personal breathing protective equipment.

Action Items

  • All stakeholders should familiarise themselves with the full text of the regulation and the associated Annex.

Key Entities Referenced

European Commission: The executive branch of the European Union, responsible for proposing legislation, implementing decisions, and managing the day-to-day business of the EU. European Food Safety Authority (EFSA): Provides independent scientific advice on risks related to food and feed safety. AB Enzymes Finland Oy: The holder of authorisation for the 6-phytase feed additive. Regulation (EC) No 1831/2003: Regulation of the European Parliament and of the Council on additives for use in animal nutrition. Commission Regulation (EC) No 378/2005: Commission Regulation on detailed rules for the implementation of Regulation (EC) No 1831/2003 as regards the duties and tasks of the Community Reference Laboratory concerning applications for authorisations of feed additives. Trichoderma reesei CBS 126897: The specific strain of Trichoderma reesei used to produce the 6-phytase enzyme.
Official Source Record View Original Source →
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Official Journal EN of the European Union L series 2025/142 30.1.2025 COMMISSION IMPLEMENTING REGULATION (EU) 2025/142 of 29 January 2025 concerning the authorisation of a preparation of 6-phytase produced with Trichoderma reesei CBS 126897 as a feed additive for fin fish (holder of authorisation: AB Enzymes Finland Oy) (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 2003on additives for use in animal nutrition(1), and in particular Article 9(2) thereof, Whereas: (1) Regulation (EC) No 1831/2003 provides for the authorisation of additives for use in animal nutrition and for the grounds and procedures for granting such an authorisation. (2) In accordance with Article 7 of Regulation (EC) No 1831/2003, an application was submitted for the authorisation of a preparation of 6-phytase produced with Trichoderma reesei CBS 126897. That application was accompanied by the particulars and documents required under Article 7(3) of Regulation (EC) No 1831/2003. (3) The application concerns the authorisation of the preparation of 6-phytase produced with Trichoderma reesei CBS 126897 as a feed additive for fin fish, requesting that additive to be classified in the category ‘zootechnical additives’ and in the functional group ‘digestibility enhancers’. (4) The European Food Safety Authority (‘the Authority’) concluded in its opinion of 12 March 2024(2)that, under the proposed conditions of use, the preparation of 6-phytase produced with Trichoderma reesei CBS 126897 is safe for fin fish. It further stated that the preparation is safe for consumers and the environment. The Authority also concluded that the preparation of 6-phytase produced with Trichoderma reesei CBS 126897, in all formulations of the additive, is neither considered a skin or eye irritant nor a skin sensitiser but is considered a respiratory sensitiser. The Authority further concluded that the preparation of 6-phytase produced with Trichoderma reesei CBS 126897 has the potential to be efficacious for salmonids and ornamental fish at 500 FTU/kg complete feed and for other fin fish at 2 500 FTU/kg complete feed. It did not consider that there is a need for specific requirements of post-market monitoring. (5) In accordance with Article 5(4), point (a), of Commission Regulation (EC) No 378/2005(3), the Reference Laboratory set up by Regulation (EC) No 1831/2003 considered that the conclusions and recommendations reached in a previous assessment concerning the same additive are valid and applicable for the current application. (6) In view of the above, the Commission considers that the preparation of 6-phytase produced with Trichoderma reesei CBS 126897 satisfies the conditions for authorisation provided for in Article 5 of Regulation (EC) No 1831/2003. Accordingly, the use of that preparation should be authorised for fin fish. In addition, the Commission considers that appropriate protective measures should be taken to prevent adverse effects on the health of the users of the additive. (1) OJ L 268, 18.10.2003, p. 29, ELI: http://data.europa.eu/eli/reg/2003/1831/oj. (2) EFSA Journal. 2024;22:e8709. (3) Commission Regulation (EC) No 378/2005 of 4 March 2005 on detailed rules for the implementation of Regulation (EC) No 1831/2003 of the European Parliament and of the Council as regards the duties and tasks of the Community Reference Laboratory concerning applications for authorisations of feed additives (OJ L 59, 5.3.2005, p. 8, ELI: http://data.europa.eu/eli/reg/ 2005/378/oj). ELI: http://data.europa.eu/eli/reg_impl/2025/142/oj 1/3EN OJ L, 30.1.2025 (7) 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 Authorisation The preparation specified in the Annex, belonging to the additive category ‘zootechnical additives’ and to the functional group ‘digestibility enhancers’, is authorised as an additive in animal nutrition, subject to the conditions laid down in that Annex. Article 2 Entry into force This Regulation shall enter into force on the twentieth 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, 29 January 2025. For the Commission The President Ursula VON DER LEYEN 2/3 ELI: http://data.europa.eu/eli/reg_impl/2025/142/ojANNEX Identifi- Minimum Maximum cation Name of the Species or content content End of period Composition, chemical formula, Maximum number holder of Additive description, analytical method category of age Units of activity/kg of Other provisions of of the feed authorisation animal complete feedingstuff with a authorisation additive moisture content of 12 % Category: zootechnical additives. Functional group: digestibility enhancers 4a19 AB Enzymes 6-phytase (EC Additive composition Salmonids — 500 FTU — 1. In the directions for use of the 19 February Finland Oy 3.1.3.26) Preparation of 6-phytase additive and premixtures, the 2035 Ornamental produced with Trichoderma reesei storage conditions and fish CBS 126897 having a minimum stability to heat treatment shall activity of: 5 000FTU(1)/g. Other fin fish 2 500FTU be indicated. Solid forms and liquid forms 2. For users of the additive and Characterisation of the active premixtures, feed business substance operators shall establish 6-phytase (EC 3.1.3.26) produced operational procedures and with Trichoderma reesei CBS organisational measures to 126897 address the potential risks Analytical method(2) resulting from their use. For the determination of Where those risks cannot be 6-phytase in the feed additive, eliminated by such procedures premixtures and compound feed: and measures, the additive and — colorimetric method based premixtures shall be used with on the enzymatic reaction personal breathing protective of 6-phytase on the phytate – equipment. EN ISO 30024. (1) One phytase unit (FTU) is the quantity of enzyme that liberates 1 μmol of inorganic phosphate per minute from sodium phytate at 37 °C, pH 5,5, under standard assay conditions. (2) Details of the analytical methods are available at the following address of the Reference Laboratory: https://joint-research-centre.ec.europa.eu/eurl-fa-eurl-feed-additives/eurl-fa-authorisation/eurl-fa- evaluation-reports_en ELI: http://data.europa.eu/eli/reg_impl/2025/142/oj 3/3 OJ L, 30.1.2025 EN

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