Commission Implementing Regulation (EU) 2025/2606
This regulation standardizes how Member States report on their implementation of the Clean Vehicles Directive (2009/33/EC). It sets out a uniform format to ensure consistent and comparable reporting across the EU. The reporting template focuses on the number and categories of clean road transport vehicles procured under public contracts, the measures taken to implement the Directive, and future activities planned. Member States must report on their institutional setup, quantitative data from both EU and national sources, and qualitative information on the Directive’s implementation. The goal is to help the Commission monitor progress towards EU low-emission mobility goals.
Commission Implementing Regulation (EU) 2025/2603
This regulation updates the representative import prices for certain poultry and egg products from Brazil by amending Regulation (EC) No 1484/95. The adjustments to these prices and associated security deposits are designed to accurately reflect current market conditions. This impacts importers and customs authorities directly, ensuring that import duties align with market fluctuations. The updated Annex specifies the CN code, product description (frozen chicken legs and cuts), representative price, security deposit, and country of origin (Brazil).
Commission Implementing Regulation (EU) 2025/2629
This regulation amends Implementing Regulation (EU) 2023/594 by updating the restricted zones (I, II, and III) and infected zones in various Member States due to the evolving situation with African Swine Fever (ASF). Annex I outlines restricted zones in Germany, Estonia, Latvia, Hungary, Poland, Slovakia, Italy, Czechia, Greece, Croatia, and Lithuania, specifying geographic areas where special control measures apply. Annex II lists areas established as infected zones, including new outbreaks in Spain and Poland. It also repeals Implementing Decision (EU) 2025/2489, which had established interim emergency measures for Spain. Anyone involved in the movement of live pigs and pork products must take note of these zones, as they are key for trade regulations.
Commission Implementing Regulation (EU) 2025/2589
This regulation imposes a definitive anti-dumping duty on imports of choline chloride originating from the People’s Republic of China, following an investigation that determined the Union industry suffered injury due to dumping. It specifies duty rates for individual Chinese exporting producers and for all other imports from China. The regulation defines the product concerned, calculates dumping margins, assesses injury to the Union industry, and establishes a causal link between dumped imports and injury. It also addresses the Union interest and determines the level of anti-dumping measures. Importers need to pay attention to the specific duty rates for different companies, and all importers need a valid commercial invoice.
Commission Implementing Regulation (EU) 2025/2581
This regulation expands the list of Combined Nomenclature (CN) and TARIC codes for pea protein imports from China that are subject to registration. This amendment to Implementing Regulation (EU) 2025/2144 ensures that all relevant categories of pea protein, specifically those with more than 65% protein on a dry weight basis, are registered by customs authorities. Businesses importing pea protein from China should review the updated list of codes to comply with EU customs regulations.
Commission Implementing Regulation (EU) 2025/2576
This regulation authorizes a preparation containing Bacillus subtilis DSM 32324, Bacillus subtilis DSM 32325, and Bacillus amyloliquefaciens DSM 25840 as a feed additive for all poultry species for laying or breeding. It also updates the authorization terms for the same preparation used for poultry species for fattening or rearing, particularly regarding a new formulation with a 10-fold increased concentration of the active agents. Feed business operators must establish operational procedures and use protective equipment. The authorization is valid until 27 November 2035.
Commission Implementing Regulation (EU) 2025/2566
This regulation authorizes the use of L-lysine sulphate and L-lysine monohydrochloride, both produced with Corynebacterium glutamicum CGMCC 7.453, as feed additives for all animal species. A maximum content of 10,000 mg/kg of complete feed is set for L-lysine sulphate. The additives must be rumen-protected when fed to ruminants. Feed business operators need to take note of specific labeling requirements to prevent nutritional imbalances and operational procedures to mitigate inhalation risks.
Commission Implementing Regulation (EU) 2025/2615
This regulation updates the animal health certificates for the re-entry of registered horses into the EU after competing in specific events, including adding a show jumping event in Canada. The updated certificate (“EQUI-RE-ENTRY-90-COMP”) and declaration are now in Chapter 16 of Annex II to Implementing Regulation (EU) 2021/403. It applies only to horses returning within 90 days after competing in events such as the Olympics, World Equestrian Games, and specified events in Mexico, the United States, Canada, China and the United Arab Emirates. The official veterinarian must attest to the horse’s health, and the operator must declare details of the horse’s export and health status. The regulation allows for continued use of certificates issued under the previous regulation until October 8, 2026.
Commission Implementing Regulation (EU) 2025/2590
This regulation authorizes the use of L-valine produced with Corynebacterium glutamicum KCCM 80365 as a feed additive for all animal species. The authorization is valid until 8 January 2036. The directions for use must specify storage conditions, heat treatment stability, and stability in water. L-valine must be rumen-protected when fed to ruminants, and the label must caution about potential nutritional imbalances.
Commission Implementing Regulation (EU) 2025/2575
This regulation withdraws specific feed additives from the market because their re-evaluation applications were absent or withdrawn. Existing stocks of these additives, premixtures, and feed materials can be used until January 8, 2028, following specific transitional measures. Feed manufacturers and users should carefully review the Annex to identify the additives being withdrawn and adjust their formulations accordingly.
Commission Implementing Regulation (EU) 2025/2573
This regulation amends Regulation (EC) No 440/2008, updating test methods for the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) to align with technical progress and reduce animal testing. The updated test methods include revised OECD test guidelines for skin sensitization, eye damage, and ecotoxicity. The inclusion of new and revised OECD test guidelines provide more accurate and reliable ways to assess the potential risks of chemical substances to human health and the environment, while also aiming to reduce animal testing.
Review of each of legal acts published today:
Commission Implementing Regulation (EU) 2025/2606 of 18 December 2025 setting out the format of Member State reports on the implementation of Directive 2009/33/EC of the European Parliament and of the Council
This Commission Implementing Regulation (EU) 2025/2606 establishes a standardized format for Member States to report on their implementation of Directive 2009/33/EC, which promotes clean road transport vehicles. The regulation aims to ensure consistent and comparable reporting across the EU, focusing on the number and categories of vehicles procured under public contracts, implementation measures, and future activities. This will enable the Commission to effectively monitor progress towards low-emission mobility goals.
The Regulation consists of two articles and an annex. Article 1 defines that the template for the reports on the implementation of Directive 2009/33/EC is set out in the Annex. Article 2 states that the regulation enters into force on the twentieth day following its publication in the Official Journal of the European Union. The Annex provides a detailed template for the report, divided into four main sections: Institutional Setup and Transposition, Quantitative data from the Tender Electronic Daily (TED) database and eForms, Quantitative data from national sources, and Qualitative information on the implementation of the Directive. The template includes specific tables for reporting data extracted from the TED database and eForms, as well as data from national monitoring schemes.
The most important provisions for Member States are those outlined in the Annex, which detail the specific information required in each section of the report. Member States must provide an overview of the authorities responsible for implementation, how minimum procurement targets are applied, and whether any national exemptions are used. They must also report quantitative data on vehicle procurement, including the number of clean vehicles, using data from both EU-level (TED) and national sources. Finally, Member States must provide qualitative information on implementation measures, identified barriers, and future activities.
Commission Implementing Regulation (EU) 2025/2603 of 12 December 2025 amending Regulation (EC) No 1484/95 as regards fixing representative prices in the poultrymeat and egg sectors and for egg albumin
This Commission Implementing Regulation (EU) 2025/2603 amends Regulation (EC) No 1484/95, which sets out rules for additional import duties and representative prices in the poultry and egg sectors. The new regulation updates the representative import prices for certain poultry and egg products and egg albumin to reflect price variations based on their origin. This adjustment ensures that import duties accurately reflect current market conditions.
The regulation consists of two articles and an annex. Article 1 stipulates that Annex I of Regulation (EC) No 1484/95 is replaced by the text in the annex of this new regulation. Article 2 states that the regulation comes into force on the day of its publication in the Official Journal of the European Union. The annex contains a table specifying the CN code, description of the product (Fowls of the species Gallus domesticus, legs and cuts thereof, frozen), representative price, security under Article 3, and the origin (Brazil) for the listed poultry product.
The most important provision is the updated Annex I, which directly impacts importers and customs authorities by changing the representative prices and security deposits for specific poultry products from Brazil. This change is crucial for calculating import duties and ensuring fair trade practices within the EU.
Commission Implementing Regulation (EU) 2025/2629 of 18 December 2025 amending Annexes I and II to Implementing Regulation (EU) 2023/594 laying down special control measures for African swine fever and repealing Commission Implementing Decision (EU) 2025/2489 concerning certain interim emergency measures relating to African swine fever in Spain
Okay, here’s a breakdown of Commission Implementing Regulation (EU) 2025/2629:
**1. Essence of the Act:**
This regulation amends Implementing Regulation (EU) 2023/594, which lays down special control measures for African swine fever (ASF). The changes involve updating the lists of restricted zones (I, II, and III) in Annex I and infected zones in Annex II based on the evolving epidemiological situation of ASF in several Member States. It also repeals Implementing Decision (EU) 2025/2489, which contained interim emergency measures for Spain.
**2. Structure and Main Provisions:**
* **Article 1:** This article is the core of the amendment. It replaces Annexes I and II of the original Implementing Regulation (EU) 2023/594 with the updated versions provided in the Annex to this new regulation. Annex I lists restricted zones I, II, and III in various Member States (Germany, Estonia, Latvia, Hungary, Poland, Slovakia, Italy, Czechia, Greece, Croatia, Lithuania), specifying geographical areas where special control measures apply. Annex II lists areas established as infected zones following outbreaks of ASF in previously disease-free regions.
* **Article 2:** This repeals Commission Implementing Decision (EU) 2025/2489, which had set out interim emergency measures for Spain following an ASF outbreak.
* **Article 3:** This specifies that the regulation comes into force the day after its publication in the Official Journal of the European Union.
**Changes Compared to Previous Versions:**
The regulation modifies the geographical boundaries and classifications of restricted zones in several countries (Hungary, Italy, Latvia, Lithuania, Poland) based on recent outbreaks and improvements in the ASF situation. It also adds new infected zones in Spain and Poland to Annex II, reflecting the spread of the disease to previously unaffected areas.
**3. Main Provisions Important for Use:**
* **Annex I (Restricted Zones):** This is crucial for anyone involved in the movement of live pigs, pork, or related products. It defines the areas where restrictions apply, and businesses need to be aware of these zones to comply with trade and movement regulations. The zones are categorized (I, II, III) with varying levels of restrictions.
* **Annex II (Infected Zones):** This is important for Member States and stakeholders in newly affected regions. Listing as an infected zone triggers specific disease control measures to prevent further spread.
* The regulation emphasizes that the zoning is based on the epidemiological situation, risk assessments, scientifically agreed principles, and international standards.
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This regulation has implications for Ukraine, as African Swine Fever is a significant concern in the region. Ukrainians involved in pig farming or trade with the EU need to be aware of these restrictions to ensure compliance and prevent the spread of the disease.
Commission Implementing Regulation (EU) 2025/2589 of 18 December 2025 imposing a definitive anti-dumping duty and definitively collecting the provisional duty imposed on imports of choline chloride originating in the People’s Republic of China
This is Commission Implementing Regulation (EU) 2025/2589 imposing a definitive anti-dumping duty on imports of choline chloride originating in the People’s Republic of China. The regulation follows an anti-dumping investigation initiated in response to a complaint by Union producers, and it confirms the imposition of definitive anti-dumping duties after a provisional duty was already in place. The regulation specifies the rates of duty for various Chinese exporting producers and for all other imports from China, aiming to protect the Union industry from the injurious effects of dumping. It also addresses claims and comments made by interested parties during the investigation, clarifying the scope of the product concerned and the methodology used to determine dumping and injury.
The structure of the act is as follows:
* **Section 1 (Procedure):** Details the initiation of the investigation, registration of imports, imposition of provisional measures, and subsequent procedures, including comments from interested parties.
* **Section 2 (Product Concerned and Like Product):** Defines the product under investigation (choline chloride) and addresses claims regarding the product scope, specifically whether to exclude choline chloride destined for food applications.
* **Section 3 (Dumping):** Explains the calculation of the normal value, the existence of significant distortions in the People’s Republic of China, the choice of a representative country, factors of production, export price, comparison, and dumping margins.
* **Section 4 (Injury):** Defines the Union industry, Union consumption, imports from the country concerned, and the economic situation of the Union industry, ultimately concluding on the injury suffered.
* **Section 5 (Causation):** Establishes the causal link between the dumped imports and the injury to the Union industry, considering other potential factors.
* **Section 6 (Level of Measures):** Determines the injury margin and the appropriate level of anti-dumping measures.
* **Section 7 (Union Interest):** Assesses the impact of the measures on the Union industry, unrelated importers, and users, concluding on the overall Union interest.
* **Section 8 (Definitive Anti-Dumping Measures):** Imposes definitive anti-dumping measures, addresses a proposal for a tariff rate quota, and specifies the duty rates.
* **Section 9 (Final Provision):** Includes a provision regarding the interest to be paid in case of reimbursement following a judgment of the Court of Justice of the European Union.
Compared to the provisional regulation, this implementing regulation confirms and adjusts certain findings based on comments received from interested parties. Key changes include:
* Adjustments to dumping margins for specific companies based on revised calculations.
* Clarifications regarding the inclusion of food grade choline chloride within the product scope.
* Revisions to the calculation of CIF prices and underselling margins.
The main provisions of the act that may be the most important for its use are:
* **Article 1:** Imposes the definitive anti-dumping duty on imports of choline chloride originating in the People’s Republic of China. It specifies the duty rates for named companies and for all other imports, as well as the conditions for applying individual duty rates, including the requirement for a valid commercial invoice with a specific declaration.
* **Article 2:** States that the amounts secured by way of the provisional anti-dumping duty shall be definitively collected, with excess amounts released.
* **Article 3:** Provides a mechanism for new exporting producers from the People’s Republic of China to be added and made subject to the appropriate weighted average anti-dumping duty rate for cooperating companies not included in the sample, under certain conditions.
* **Article 4:** Specifies the date of entry into force of the regulation.
Commission Implementing Regulation (EU) 2025/2581 of 18 December 2025 amending Implementing Regulation (EU) 2025/2144 making imports of pea protein originating in the People’s Republic of China subject to registration
This Commission Implementing Regulation (EU) 2025/2581 amends Implementing Regulation (EU) 2025/2144, which made imports of pea protein from China subject to registration. The amendment expands the list of Combined Nomenclature (CN) and TARIC codes under which pea protein imports are to be registered. This adjustment is necessary because, during the anti-dumping investigation, additional CN codes relevant to the product under investigation were identified.
The regulation consists of two articles. Article 1 replaces the original Article 1 of Implementing Regulation (EU) 2025/2144 with an updated list of CN and TARIC codes for high protein content pea protein (more than 65% protein on a dry weight basis) that customs authorities must register when imported from China. Article 2 stipulates that the regulation comes into force the day after its publication in the Official Journal of the European Union and is binding in its entirety and directly applicable in all Member States. The key change is the expanded list of CN and TARIC codes, ensuring that all relevant categories of pea protein imports are subject to registration.
The most important provision is the revised list of CN and TARIC codes in Article 1. Businesses involved in importing pea protein from China need to be aware of these updated codes to ensure compliance with EU customs regulations. The inclusion of these additional codes means that a broader range of pea protein products will now be subject to registration, which is a critical step in the EU’s anti-dumping investigation.
Commission Implementing Regulation (EU) 2025/2576 of 18 December 2025 concerning the authorisation of a preparation of Bacillus subtilis DSM 32324, Bacillus subtilis DSM 32325 and Bacillus amyloliquefaciens DSM 25840 as a feed additive for all poultry species for laying or for breeding (holder of authorisation: Chr. Hansen A/S) and amending Implementing Regulation (EU) 2020/1762 as regards the terms of the authorisation of a preparation of Bacillus subtilis DSM 32324, Bacillus subtilis DSM 32325 and Bacillus amyloliquefaciens DSM 25840 as a feed additive for all poultry species for fattening or reared for laying or reared for breeding
This Commission Implementing Regulation (EU) 2025/2576 concerns the authorization of a preparation of Bacillus subtilis DSM 32324, Bacillus subtilis DSM 32325, and Bacillus amyloliquefaciens DSM 25840 as a feed additive for all poultry species for laying or breeding. It also amends Implementing Regulation (EU) 2020/1762 to update the terms of authorization for the same preparation when used for all poultry species for fattening or reared for laying or breeding, specifically regarding a new formulation with a 10-fold increased concentration of the active agents. The additive is classified as a zootechnical additive and functions as a gut flora stabilizer.
The regulation consists of four articles and two annexes. Article 1 authorizes the use of the specified preparation as a feed additive under the conditions outlined in Annex I. Article 2 replaces the annex of Implementing Regulation (EU) 2020/1762 with Annex II of this new regulation, updating the terms for using the additive in poultry for fattening or rearing. Article 3 provides transitional measures, allowing the continued use and marketing of the additive and related products produced and labeled before specific dates, until stocks are exhausted. Article 4 states that the regulation will enter into force twenty days after its publication in the Official Journal of the European Union.
The main change introduced by this regulation is the authorization of the feed additive for poultry species for laying or breeding, in addition to its already authorized use for poultry species for fattening or rearing. Furthermore, it introduces a new formulation of the additive with a higher concentration of active agents (3,2 × 1010 CFU/g additive), and updates safety measures, requiring feed business operators to establish operational procedures and organizational measures to address potential risks, including the use of personal protective equipment where risks cannot be eliminated.
Commission Implementing Regulation (EU) 2025/2566 of 18 December 2025 concerning the authorisation of L-lysine sulphate and L-lysine monohydrochloride produced with Corynebacterium glutamicum CGMCC 7.453 as feed additives for all animal species
This Commission Implementing Regulation (EU) 2025/2566 authorises the use of L-lysine sulphate and L-lysine monohydrochloride, both produced with Corynebacterium glutamicum CGMCC 7.453, as feed additives for all animal species. These additives are classified as ‘nutritional additives’ within the functional group of ‘amino acids, their salts and analogues’. The regulation specifies conditions for use, including maximum content levels and labeling requirements, and ensures the safety and efficacy of these additives in animal nutrition.
The regulation consists of two articles and an annex. Article 1 states that the substances specified in the Annex are authorised as additives in animal nutrition, subject to the conditions laid down in that Annex. Article 2 indicates the date of entry into force of the regulation. The Annex specifies the identification number, name, composition, analytical method, animal species, and other provisions for L-lysine sulphate and L-lysine monohydrochloride. It sets a maximum content for L-lysine sulphate and outlines requirements for labeling, use in water for drinking, and protection against degradation in the rumen for ruminants.
Key provisions include the authorisation of L-lysine sulphate and L-lysine monohydrochloride for all animal species, with specific conditions for their use. A maximum content of 10,000 mg/kg of complete feed is set for L-lysine sulphate. The regulation mandates that feed business operators ensure L-lysine sulphate and L-lysine monohydrochloride are rumen protected when fed to ruminants. It also requires specific labeling to address potential nutritional imbalances and the establishment of operational procedures to mitigate inhalation risks for users of the additives.
Commission Implementing Regulation (EU) 2025/2615 of 17 December 2025 amending Annex II to Implementing Regulation (EU) 2021/403 as regards the model animal health certificate and the model declaration for the re-entry into the Union of registered horses for competition
This is a description of Commission Implementing Regulation (EU) 2025/2615, which amends Annex II to Implementing Regulation (EU) 2021/403 regarding animal health certificates for the re-entry of registered horses into the EU after competing in certain events. The regulation updates the model animal health certificate and declaration required for horses returning to the EU after temporary export for competition, specifically to include a show jumping event in Canada. It aims to ensure clarity and consistency in EU rules for the re-entry of these horses.
**Structure and Main Provisions:**
* **Amendment of Annex II:** The core of the regulation is the replacement of Chapter 16 of Annex II to Implementing Regulation (EU) 2021/403 with a new version. This chapter contains the model animal health certificate (“EQUI-RE-ENTRY-90-COMP”) and the model declaration for the re-entry of registered horses.
* **Inclusion of Canadian Event:** The updated certificate and declaration now explicitly include the show jumping event (Concours de Saut International 5*) taking place in Canada within the list of eligible equestrian events.
* **Updated References and Structure:** The new models feature updated references, notes, and structural elements for improved clarity and compliance.
* **Transitional Period:** To avoid disruption, the regulation allows for the continued use of certificates and declarations issued under the previous version of Implementing Regulation (EU) 2021/403 until October 8, 2026, provided they were issued no later than July 8, 2026.
**Main Provisions for Use:**
* **Specific Events:** The certificate “EQUI-RE-ENTRY-90-COMP” is applicable only for horses re-entering the EU after temporary export for participation in specific equestrian events organized under the auspices of the Fédération Equestre Internationale (FEI), including the Olympic Games, World Equestrian Games, Asian Equestrian Games, American Equestrian Games, and specified show jumping and dressage events in Mexico, the United States, Canada, China and the United Arab Emirates.
* **90-Day Limit:** The temporary export period must not exceed 90 days.
* **Health Requirements:** The certificate requires attestation by an official veterinarian regarding the horse’s health status, including clinical examinations and compliance with disease-related requirements.
* **Declaration by Operator:** The operator responsible for the horse must sign a declaration confirming details of the horse’s export, participation in eligible events, health status, and compliance with transportation and isolation conditions.
* **Third Country/Territory of Origin:** The certificate requires information about the third country or territory of origin, including its disease status and Sanitary Group classification.
* **Residence and Isolation:** The certificate includes attestations regarding the horse’s residence and isolation prior to dispatch to the Union, including requirements for accommodation in separated stables and contact with other horses.
Commission Implementing Regulation (EU) 2025/2590 of 18 December 2025 concerning the authorisation of L-valine produced with Corynebacterium glutamicum KCCM 80365 as a feed additive for all animal species
This Commission Implementing Regulation (EU) 2025/2590 authorises the use of L-valine produced with Corynebacterium glutamicum KCCM 80365 as a feed additive for all animal species. The additive is classified as a nutritional additive, specifically an amino acid, its salt, or analogue. The regulation sets conditions for its use, including requirements for proper labeling, storage, and application, particularly when used in water for drinking or fed to ruminants. The authorisation is valid until 8 January 2036.
The regulation consists of two articles and an annex. Article 1 authorises the substance specified in the Annex as an additive in animal nutrition, subject to the conditions laid down in that Annex. Article 2 states that the regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union. The Annex specifies the identification number, name, composition, analytical method, animal species, and other provisions for the use of L-valine as a feed additive. There are no direct comparisons to previous versions, as this appears to be the initial authorisation for this specific use of L-valine produced with Corynebacterium glutamicum KCCM 80365.
The most important provisions for users include the requirement to indicate storage conditions, heat treatment stability, and stability in water for drinking in the directions for use. The regulation explicitly allows the additive to be used via water for drinking but requires feed business operators to ensure that L-valine is rumen-protected when fed to ruminants. Furthermore, the label must indicate the need to consider all essential and conditionally essential amino acids to avoid nutritional imbalances, especially when supplementing with L-valine via water for drinking.
Commission Implementing Regulation (EU) 2025/2575 of 18 December 2025 withdrawing from the market certain feed additives
This Commission Implementing Regulation (EU) 2025/2575 mandates the withdrawal of specific feed additives from the market due to the absence or withdrawal of applications for their re-evaluation as required by Regulation (EC) No 1831/2003. This action ensures that only additives with up-to-date safety and efficacy assessments are available for use in animal nutrition. The regulation also addresses transitional measures for using existing stocks of the affected additives.
The regulation is structured with:
* **Article 1:** Specifies that the feed additives listed in the Annex must be withdrawn from the market for the animal species and categories detailed in the Annex.
* **Article 2:** Amends Regulation (EC) No 358/2005 by deleting entry 28 concerning 3-Phytase EC 3.1.3.8 from Annex III.
* **Article 3:** Repeals Regulations (EC) No 316/2003, (EC) No 1811/2005, and (EC) No 1876/2006.
* **Article 4:** Establishes transitional measures, allowing existing stocks of the listed feed additives to be placed on the market and used until January 8, 2027. Premixtures produced with these additives can be marketed and used until April 8, 2027, and compound feed and feed materials produced with these additives or premixtures can be marketed and used until January 8, 2028.
* **Article 5:** Sets the entry into force of the Regulation as the twentieth day following its publication in the Official Journal of the European Union.
* **Annex:** Lists the specific feed additives to be withdrawn from the market, categorized by whether they were authorized without a time limit (Chapter I.A) or for a limited period (Chapter I.B), and specifies the animal species and categories affected by the withdrawal.
Compared to previous regulations, this act consolidates the withdrawal of several feed additives under a single regulation, streamlining the process and ensuring consistency in the application of Regulation (EC) No 1831/2003. It repeals several older regulations that authorized the use of these additives, reflecting the updated status based on the re-evaluation process.
The most important provisions for practical use are:
* **Article 1 and the Annex:** These sections clearly identify which feed additives are being withdrawn and for which animal species or categories. This is crucial for manufacturers and users of feed to ensure compliance.
* **Article 4 (Transitional Measures):** This article provides a timeline for using up existing stocks of the affected additives, premixtures, and feed materials. This is essential for businesses to manage their inventory and adjust their formulations to comply with the new regulation without incurring unnecessary losses.
Commission Regulation (EU) 2025/2573 of 18 December 2025 amending Regulation (EC) No 440/2008 as regards the test methods, to adapt them to technical progress
This is a description of Commission Regulation (EU) 2025/2573, which amends Regulation (EC) No 440/2008 regarding test methods for the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH). The amending regulation updates the test methods to align with technical progress and reduce animal testing. It incorporates updated and new test methods developed by the Organisation for Economic Co-operation and Development (OECD).
The regulation modifies the Annex to Regulation (EC) No 440/2008. These changes include updating test methods for human health effects related to eye damage/irritation and skin sensitization, as well as adding new test methods for assessing ecotoxicity. Furthermore, it updates and corrects several OECD Test Guidelines and adds new test methods relevant for assessing the dustiness of nanoforms of substances. Finally, it removes outdated full descriptions of certain test methods, referencing the updated versions in Part 0 of the Annex.
The most important provisions of this regulation are the updated test methods for assessing the potential hazards of chemical substances. Specifically, the inclusion of new and revised OECD test guidelines for in vitro skin sensitization assays (OECD Test Guidelines 442C, 442D, and 442E), defined approaches for eye damage and irritation (OECD Test Guideline 467), in vitro macromolecular test method for identifying chemicals inducing serious eye damage (OECD Test Guideline 496), the Rapid Estrogen Activity In Vivo (REACTIV) assay (OECD Test Guideline 252), the Short-term Juvenile Hormone Activity Screening Assay using Daphnia magna (JHASA) (OECD Test Guideline 253), and the Hyallela azteca Bioconcentration Test (HYBIT) (OECD Test Guideline 321). These updated and new methods provide more accurate and reliable ways to assess the potential risks of chemical substances to human health and the environment, while also aiming to reduce animal testing.
