EU Legal Acts Review<\/title><br \/>\n<\/head><\/p>\n<h4>Review of EU Legal Acts<\/h4>\n<h5>Commission Delegated Regulation (EU) 2025\/2004<\/h5>\n<p>This regulation modifies existing rules on bluefin tuna catch documentation. Key changes include simplified reporting requirements for Member States regarding derogations on intra-EU trade, making it easier for the Commission to track trade verification and outcomes. Additionally, it streamlines the process for determining the weight of individual bluefin tuna, especially in fisheries with minimum conservation reference size derogations, by allowing the use of average weight based on total landing weight.<\/p>\n<h5>Commission Delegated Regulation (EU) 2025\/2002<\/h5>\n<p>This regulation tightens the management of fish aggregating devices (FADs) used in tuna fishing within the ICCAT Convention area. It specifically reduces the number of FADs allowed per vessel to 288, down from the previous limit of 300. This aims to promote the long-term conservation and sustainable use of Atlantic fishery resources.<\/p>\n<h5>Commission Delegated Regulation (EU) 2025\/2017<\/h5>\n<p>This regulation updates the compositional requirements for infant and follow-on formula, particularly those made from protein hydrolysates. It introduces a new “Protein-related requirements group E,” setting specific criteria for formulas using a specific protein hydrolysate evaluated by the European Food Safety Authority (EFSA). Manufacturers using this particular protein hydrolysate must now comply with these detailed requirements, covering protein content, source, processing, and amino acid composition.<\/p>\n<h5>Directive (EU) 2025\/2482<\/h5>\n<p>This Directive overhauls the River Information Services (RIS) framework to bolster the safety, efficiency, and sustainability of inland waterway transport within the EU. It hones in on harmonising and making RIS interoperable across Member States, particularly on the trans-European transport network (TEN-T). It seeks to integrate inland waterway transport more seamlessly with other transport modes through digital solutions and data sharing, and establishes a European RIS Environment to streamline information access. The focus is on modernizing RIS to enhance digital integration and data accessibility.<\/p>\n<h5>Directive (EU) 2025\/2456<\/h5>\n<p>This directive streamlines the chemical safety assessment process by shifting responsibilities to the European Chemicals Agency (ECHA). The primary goal is to improve transparency, ease burdens on stakeholders, expedite decision-making, and ensure consistency in scientific evaluations. The directive aims to enhance the evaluation process for applications for exemptions from substance restrictions and the review of substances for potential restriction. It modernises the scientific assessment of chemicals to align with ECHA’s existing standards.<\/p>\n<h5>Commission Implementing Regulation (EU) 2025\/2540<\/h5>\n<p>This regulation establishes a detailed plan for peer review of national cybersecurity certification authorities (NCCAs). It aims to ensure consistent standards for European cybersecurity certificates by setting out a schedule, frequency, and methodology for peer reviews conducted by NCCAs from different Member States and the European Commission. Key elements include a rotation system for peer reviewers, criteria for team composition, guidelines for the review process, and requirements for the peer-review report. The objective is to build confidence in cybersecurity certifications across the EU by standardizing the assessment of NCCAs.<\/p>\n<h3><strong>Review of each of legal acts published today:<\/strong><\/h3>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2004\"><\/p>\n<h3><strong>Commission Delegated Regulation (EU) 2025\/2004 of 6\u00a0October 2025 amending Regulation (EU)\u00a02023\/2833 of the European Parliament and of the Council as regards derogations on reporting of intra-EU trade and certain tagging information, and the determination of weight of individual bluefin tuna<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This Commission Delegated Regulation (EU) 2025\/2004 amends Regulation (EU) 2023\/2833, which establishes a catch documentation program for bluefin tuna. The amendments address specific derogations on reporting intra-EU trade and certain tagging information, and they also change how the weight of individual bluefin tuna is determined. These changes are made in response to recommendations from the International Commission for the Conservation of Atlantic Tunas (ICCAT).<\/p>\n<p>The regulation consists of two articles. Article 1 outlines the specific amendments to Regulation (EU) 2023\/2833, replacing Article 5(4) regarding annual reporting by Member States on the implementation of derogations, requiring information on verification, outcomes, and trade data. It also replaces Article 6(5) concerning the determination of the approximate weight of individual fish, allowing Member States to use the average weight of the total landing weight divided by the number of fish, particularly for fisheries with minimum conservation reference size derogations. Article 2 stipulates that the regulation will enter into force on the day following its publication in the Official Journal of the European Union.<\/p>\n<p>The most important provisions for practical use are the changes to Article 5(4) and Article 6(5) of Regulation (EU) 2023\/2833. The amendment to Article 5(4) clarifies the reporting requirements for Member States regarding derogations on intra-EU trade, ensuring that the Commission receives comprehensive data on verification processes and trade activities. The amendment to Article 6(5) simplifies the process for determining the weight of individual bluefin tuna, aligning it with current practices where all landed fish are weighed, and sampling is unnecessary.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2002\"><\/p>\n<h3><strong>Commission Delegated Regulation (EU) 2025\/2002 of 6\u00a0October 2025 amending Regulation (EU)\u00a02017\/2107 of the European Parliament and of the Council as regards the number of fish aggregating devices permitted in the Convention area of the International Commission for the Conservation of Atlantic Tunas<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This Commission Delegated Regulation (EU) 2025\/2002 amends Regulation (EU) 2017\/2107, focusing on the management, conservation, and control measures within the Convention area of the International Commission for the Conservation of Atlantic Tunas (ICCAT). The key change introduced by this regulation is a reduction in the number of fish aggregating devices (FADs) allowed per vessel, aligning EU law with the latest ICCAT recommendation. This adjustment aims to further the long-term conservation and sustainable use of fishery resources in the Atlantic.<\/p>\n<p>The regulation consists of two articles. Article 1 directly amends Article 9(4) of Regulation (EU) 2017\/2107, stipulating that, starting from January 1, 2026, Member States must ensure that no more than 288 FADs per vessel with operational buoys are active at any given time. This is a decrease from the previously allowed number of 300 FADs. Article 2 states that the regulation will enter into force on the day following its publication in the Official Journal of the European Union, ensuring its swift implementation.<\/p>\n<p>The most important provision of this regulation is the amended limit on FADs per vessel, reducing it to 288. This change directly impacts Union fishing vessels operating in the ICCAT Convention area, requiring them to adjust their fishing practices and equipment deployment strategies to comply with the new limit by January 1, 2026.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2017\"><\/p>\n<h3><strong>Commission Delegated Regulation (EU) 2025\/2017 of 8\u00a0October 2025 amending Delegated Regulation (EU)\u00a02016\/127 as regards the protein-related requirements for infant and follow-on formula manufactured from protein hydrolysates<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This Commission Delegated Regulation (EU) 2025\/2017 amends Delegated Regulation (EU) 2016\/127, specifically concerning the protein-related requirements for infant and follow-on formula manufactured from protein hydrolysates. The amendment introduces an additional set of requirements, named “Protein-related requirements group E,” to the existing compositional requirements for protein hydrolysates. This addition is based on a favorable scientific opinion from the European Food Safety Authority (EFSA) regarding the safety and suitability of a specific protein hydrolysate manufactured by Fonterra Cooperative Group Ltd.<\/p>\n<p>The regulation modifies Annexes I, II, and III of Delegated Regulation (EU) 2016\/127. It replaces points 2.3 in both Annex I (for infant formula) and Annex II (for follow-on formula) with updated sections that include the new “Protein-related requirements group E,” alongside the existing groups A, B, C, and D. Each group specifies different requirements for protein content, protein source, protein processing, and indispensable and conditionally indispensable amino acids. Additionally, Annex III is updated to reflect the inclusion of the new protein-related requirements group.<\/p>\n<p>The main provision of this regulation is the introduction of “Protein-related requirements group E,” which sets specific criteria for infant and follow-on formula manufactured using the protein hydrolysate evaluated by EFSA. This includes minimum and maximum protein content (0,48-0,67 g\/100 kJ), a defined protein source (whey protein concentrate from cow’s milk with a minimum protein content of 80%), a specific protein processing method (two-stage hydrolysis with serine endopeptidases), and requirements for indispensable and conditionally indispensable amino acids. Manufacturers intending to use the Fonterra protein hydrolysate must adhere to these specific requirements to ensure their products comply with EU regulations.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025L2482\"><\/p>\n<h3><strong>Directive (EU) 2025\/2482 of the European Parliament and of the Council of 26 November 2025 amending Directive 2005\/44\/EC on harmonised river information services (RIS) on inland waterways in the Community<\/strong><\/h3>\n<p><\/a><\/p>\n<p>Okay, here’s a breakdown of Directive (EU) 2025\/2482, amending Directive 2005\/44\/EC on harmonised river information services (RIS) on inland waterways:<\/p>\n<p>**1. Essence of the Act:**<\/p>\n<p>This Directive updates the framework for River Information Services (RIS) to improve safety, efficiency, and sustainability of inland waterway transport within the EU. It focuses on enhancing the harmonisation and interoperability of RIS across Member States, particularly along the trans-European transport network (TEN-T). The directive aims to integrate inland waterway transport more seamlessly with other modes of transport through digital solutions and data sharing. It also establishes a European RIS Environment to streamline information access and exchange.<\/p>\n<p>**2. Structure and Main Provisions:**<\/p>\n<p>The Directive amends several articles of the original Directive 2005\/44\/EC and adds new provisions. Key changes include:<\/p>\n<p>* **Scope:** The application of the Directive is now primarily focused on inland waterways and ports that are part of the TEN-T and directly connected to another Member State’s TEN-T waterways.<br \/>\n* **Definitions:** New definitions are added for terms like “trans-European transport network,” “European Reference Data Management System,” “port community system,” “smart inland waterway infrastructure system,” “European RIS Environment,” and “inland port.”<br \/>\n* **Setting up RIS:** Member States are required to implement RIS on relevant waterways and ports, ensuring data is up-to-date and accessible. They must also enable electronic ship reporting and provide notices to skippers in standardised formats.<br \/>\n* **European RIS Environment:** A key element is the establishment of a European RIS Environment, a single-point-of-access platform for RIS information. Member States must jointly create, govern, and maintain this environment. The Commission is empowered to adopt implementing acts to define its operational characteristics.<br \/>\n* **Technical Specifications:** The Directive emphasizes the importance of technical specifications for RIS, covering areas like inland ECDIS, electronic ship reporting, and vessel tracking. It introduces the concept of referencing the European Standard for River Information Services (ES-RIS) developed by CESNI.<br \/>\n* **Feedback Mechanism:** A new article mandates Member States to have a procedure for handling feedback from RIS users, submitted through the European RIS Environment.<br \/>\n* **Data Protection:** The Directive includes provisions to ensure the protection of personal data processed for RIS operations, in accordance with EU data protection regulations.<br \/>\n* **Delegated Powers:** The Commission is granted powers to adopt delegated acts to amend Annex I (minimum data requirements) and Annex III (technical specifications), under certain conditions.<br \/>\n* **Committee Procedure:** The Inland Waterway Transport Committee will assist the Commission in matters related to RIS.<\/p>\n<p>**3. Main Provisions Important for Use:**<\/p>\n<p>* **Focus on TEN-T:** The restriction of the scope to the TEN-T network means that RIS implementation is prioritised on the most important waterways for EU transport policy.<br \/>\n* **European RIS Environment:** The establishment of the European RIS Environment as a central platform for information exchange is a key development for RIS users.<br \/>\n* **Technical Specifications and ES-RIS:** The reference to the European Standard for River Information Services (ES-RIS) ensures that RIS implementation is based on up-to-date and harmonised technical standards.<br \/>\n* **Feedback Mechanism:** The feedback mechanism provides a channel for RIS users to report issues and contribute to the improvement of RIS implementation.<br \/>\n* **Data Requirements:** The minimum data requirements outlined in Annex I are crucial for ensuring that RIS users have access to essential information for navigation and voyage planning.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025L2456\"><\/p>\n<h3><strong>Directive (EU) 2025\/2456 of the European Parliament and of the Council of 26 November 2025 amending Directive 2011\/65\/EU as regards the reattribution of scientific and technical tasks to the European Chemicals Agency (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><\/p>\n<p>Directive (EU) 2025\/2456 amends Directive 2011\/65\/EU, focusing on reallocating scientific and technical responsibilities to the European Chemicals Agency (ECHA) to streamline chemical safety assessments. The core aim is to enhance transparency, reduce burdens on stakeholders, accelerate decision-making, and ensure consistency in scientific evaluations. This involves expanding ECHA’s role in evaluating applications for exemptions from substance restrictions and in reviewing substances for potential inclusion in the list of restricted substances. The directive seeks to align processes with ECHA’s current standards, promote digitalization, and improve data accessibility and interoperability, ultimately leading to cost savings and efficiency gains.<\/p>\n<p>The Directive modifies Articles 5, 6, 20, and 24 of Directive 2011\/65\/EU and introduces Articles 6a, 6b, and 6c, along with a new Annex Va. Key changes include:<\/p>\n<p>* **Reattribution of Tasks to ECHA:** ECHA is now responsible for receiving and processing applications for exemptions, verifying their completeness, and making them available to Member States and the public.<br \/>\n* **Enhanced Review Process:** The directive introduces detailed procedural steps for reviewing substances for potential inclusion in the list of restricted substances, ensuring a more transparent and thorough assessment.<br \/>\n* **Committee Involvement:** The Committee for Socioeconomic Analysis and, where relevant, the Committee for Risk Assessment, will provide opinions on exemption applications and proposed restrictions.<br \/>\n* **Public Availability of Information:** ECHA will make summaries and non-confidential versions of applications, as well as parts of the committees’ opinions, publicly available on its website.<br \/>\n* **Periodic Review of Restricted Substances:** The list of restricted substances will be reviewed at least every four years.<br \/>\n* **Harmonized Formats and Guidelines:** ECHA will establish harmonized formats and comprehensive guidelines for applications, taking into account the situation of SMEs.<br \/>\n* **Restriction Dossiers:** The requirements for restriction dossiers are specified in the new Annex Va, ensuring that they contain all necessary information for a thorough assessment.<\/p>\n<p>The most important provisions for practical use are those related to the new roles and responsibilities of the European Chemicals Agency (ECHA) in the assessment of applications for exemptions and the review of restricted substances. Economic operators need to be aware of the harmonized formats and guidelines that ECHA will provide for submitting applications. Member States should take note of the new procedures for preparing and submitting restriction dossiers.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2540\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2540 of 9\u00a0December 2025 laying down rules for the application of Regulation (EU)\u00a02019\/881 of the European Parliament and of the Council as regards the establishment of the plan for peer review<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This is a description of Commission Implementing Regulation (EU) 2025\/2540, which lays down rules for the application of Regulation (EU) 2019\/881 regarding the establishment of a plan for peer review of national cybersecurity certification authorities (NCCAs). The regulation aims to ensure equivalent standards for European cybersecurity certificates and EU statements of conformity by establishing a consistent peer review process across the Union. It outlines the schedule, frequency, and methodology for these peer reviews, involving NCCAs from different Member States and the European Commission. The regulation also addresses confidentiality, secure communication, and capacity-building aspects related to the peer review process.<\/p>\n<p>The regulation consists of 8 articles and 2 annexes.<\/p>\n<p>* **Article 1** establishes the schedule, frequency, and cost of peer reviews, with Annex I providing the specific schedule for each Member State. It allows for postponement requests in exceptional circumstances and clarifies the process for Member States with multiple NCCAs or those designating NCCAs from other Member States.<br \/>\n* **Article 2** sets up a rotation system for peer-reviewer NCCAs, ensuring that each NCCA participates in at least two peer reviews over a five-year period. It also allows for observer participation from other NCCAs and ENISA.<br \/>\n* **Article 3** outlines the criteria for the composition of the peer review team, including experience, knowledge, and independence requirements. It also establishes a process for addressing potential conflicts of interest.<br \/>\n* **Article 4** details the methodology for the peer review, including self-assessment questionnaires, documentation review, interviews, and on-site visits. It also addresses the language of cooperation and the responsibilities of the peer-reviewed NCCA.<br \/>\n* **Article 5** specifies the requirements for the peer-review report, including its content, timeline, and dissemination process. It also addresses the handling of comments from the peer-reviewed NCCA and the publication of a summary report.<br \/>\n* **Article 6** focuses on confidentiality, ensuring the protection of sensitive information obtained during the peer review process. It also mandates the deletion or destruction of documents after the final report is completed.<br \/>\n* **Article 7** tasks ENISA with analyzing the aggregated results of the peer reviews to identify lessons learned and best practices for capacity-building among NCCAs.<br \/>\n* **Article 8** states that the regulation will enter into force on the twentieth day following its publication in the Official Journal of the European Union.<br \/>\n* **Annex I** provides the schedule of NCCAs that are subject to peer review.<br \/>\n* **Annex II** describes the methodology of the peer review.<\/p>\n<p>The most important provisions for practical use are those concerning the schedule for peer reviews (Article 1 and Annex I), the criteria for peer review team composition (Article 3), the methodology for conducting the peer review (Article 4), and the requirements for the peer-review report (Article 5). These provisions provide a clear framework for NCCAs to prepare for and participate in the peer review process, ensuring a consistent and effective assessment of their cybersecurity certification activities.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2513\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2513 of 11\u00a0December 2025 concerning the authorisation of copper(II)-betaine complex as a feed additive for all animal species<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2501\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2501 of 11\u00a0December 2025 amending Implementing Regulation (EU)\u00a02021\/1165 as regards the use of certain products and substances in organic production<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2503\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2503 of 11\u00a0December 2025 concerning the authorisation of a preparation of endo-1,4-beta-xylanase, endo-1,4-beta-glucanase and xyloglucan-specific-endo-beta-1,4-glucanase produced with Trichoderma citrinoviride DSM 33578 as a feed additive for poultry other than poultry for fattening, poultry reared for laying and reared for breeding and porcine species other than sows of all Suidae species (holder of authorisation: Huvepharma EOOD)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2502\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2502 of 11\u00a0December 2025 concerning the authorisation of a preparation of protease produced with Bacillus subtilis CBS 148232 and viable spores of Bacillus velezensis NRRL B-50508, Bacillus velezensis NRRL B-50509 and Bacillus subtilis NRRL B-50510 as a feed additive for pigs for fattening of all Suidae species and weaned piglets of minor Suidae species (holder of authorisation: Genencor International B.V.)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2505\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2505 of 11\u00a0December 2025 concerning the authorisation of guanidinoacetic acid and a preparation of guanidinoacetic acid as feed additives for weaned piglets and pigs for fattening in water for drinking and for turkeys for fattening and reared for breeding in feed and water for drinking (holder of authorisation: Alzchem Trostberg GmbH), and amending Implementing Regulation (EU)\u00a02023\/2628<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2500\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2500 of 11\u00a0December 2025 concerning the authorisation of a preparation of Bacillus velezensis NRRL B-67647, Bacillus pumilus NRRL B-67648 and Bacillus licheniformis NRRL B-67649 as a feed additive for poultry for fattening and ornamental birds (holder of authorisation: S.I.Lesaffre)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2543\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2543 of 11\u00a0December 2025 concerning the denial of the renewal of the authorisation of Patent Blue V as a feed additive for non-food producing animals and repealing Implementing Regulation (EU) No\u00a0643\/2013<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2511\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2511 of 11\u00a0December 2025 concerning the authorisation of a preparation of Bacillus paralicheniformis DSM 33902 and Bacillus subtilis DSM 33903 as a feed additive for ruminants for milk production\/reproduction (holder of authorisation: Chr. Hansen\u00a0A\/S)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2498\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2498 of 11\u00a0December 2025 concerning the authorisation of 4-hydroxy-2,5-dimethylfuran-3(2H)-one as a feed additive for all animal species, except cats and dogs<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2457\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2457 of the European Parliament and of the Council of 26 November 2025 amending Regulations (EC) No 178\/2002, (EC) No 401\/2009, (EU) 2017\/745 and (EU) 2019\/1021 as regards the reattribution of scientific and technical tasks and improving cooperation among Union agencies in the area of chemicals (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2458\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2458 of the European Parliament and of the Council of 26 November 2025 on European statistics on population and housing, amending Regulation (EC) No 862\/2007 and repealing Regulations (EC) No 763\/2008 and (EU) No 1260\/2013 (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2518\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2518 of the European Parliament and of the Council of 26 November 2025 laying down additional procedural rules on the enforcement of Regulation (EU) 2016\/679 (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2509\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2509 of the European Parliament and of the Council of 26 November 2025 on the safety of toys and repealing Directive 2009\/48\/EC (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2455\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2455 of the European Parliament and of the Council of 26 November 2025 establishing a common data platform on chemicals, laying down rules to ensure that the data contained in it are findable, accessible, interoperable and reusable and establishing a monitoring and outlook framework for chemicals (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>EU Legal Acts Review Review of EU Legal Acts Commission Delegated Regulation (EU) 2025\/2004 This regulation modifies existing rules on bluefin tuna catch documentation. Key changes include simplified reporting requirements for Member States regarding derogations on intra-EU trade, making it easier for the Commission to track trade verification and outcomes. Additionally, it streamlines the process…<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_bbp_topic_count":0,"_bbp_reply_count":0,"_bbp_total_topic_count":0,"_bbp_total_reply_count":0,"_bbp_voice_count":0,"_bbp_anonymous_reply_count":0,"_bbp_topic_count_hidden":0,"_bbp_reply_count_hidden":0,"_bbp_forum_subforum_count":0,"pmpro_default_level":"","footnotes":""},"categories":[14],"tags":[],"class_list":["post-13913","post","type-post","status-publish","format-standard","hentry","category-eu-legislation-detailed","pmpro-has-access"],"acf":{"patreon-level":0},"_links":{"self":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/posts\/13913","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/comments?post=13913"}],"version-history":[{"count":0,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/posts\/13913\/revisions"}],"wp:attachment":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/media?parent=13913"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/categories?post=13913"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/tags?post=13913"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}

{"id":13913,"date":"2025-12-13T09:16:29","date_gmt":"2025-12-13T07:16:29","guid":{"rendered":"https:\/\/lexcovery.com\/2025\/12\/review-of-the-eu-legislation-for-13-12-2025\/"},"modified":"2025-12-13T09:16:29","modified_gmt":"2025-12-13T07:16:29","slug":"review-of-the-eu-legislation-for-13-12-2025","status":"publish","type":"post","link":"https:\/\/lexcovery.com\/en\/2025\/12\/review-of-the-eu-legislation-for-13-12-2025\/","title":{"rendered":"Review of the EU legislation for 13\/12\/2025"},"content":{"rendered":"

<\/p>\n

\nEU Legal Acts Review<\/title><br \/>\n<\/head><\/p>\n<h4>Review of EU Legal Acts<\/h4>\n<h5>Commission Delegated Regulation (EU) 2025\/2004<\/h5>\n<p>This regulation modifies existing rules on bluefin tuna catch documentation. Key changes include simplified reporting requirements for Member States regarding derogations on intra-EU trade, making it easier for the Commission to track trade verification and outcomes. Additionally, it streamlines the process for determining the weight of individual bluefin tuna, especially in fisheries with minimum conservation reference size derogations, by allowing the use of average weight based on total landing weight.<\/p>\n<h5>Commission Delegated Regulation (EU) 2025\/2002<\/h5>\n<p>This regulation tightens the management of fish aggregating devices (FADs) used in tuna fishing within the ICCAT Convention area. It specifically reduces the number of FADs allowed per vessel to 288, down from the previous limit of 300. This aims to promote the long-term conservation and sustainable use of Atlantic fishery resources.<\/p>\n<h5>Commission Delegated Regulation (EU) 2025\/2017<\/h5>\n<p>This regulation updates the compositional requirements for infant and follow-on formula, particularly those made from protein hydrolysates. It introduces a new “Protein-related requirements group E,” setting specific criteria for formulas using a specific protein hydrolysate evaluated by the European Food Safety Authority (EFSA). Manufacturers using this particular protein hydrolysate must now comply with these detailed requirements, covering protein content, source, processing, and amino acid composition.<\/p>\n<h5>Directive (EU) 2025\/2482<\/h5>\n<p>This Directive overhauls the River Information Services (RIS) framework to bolster the safety, efficiency, and sustainability of inland waterway transport within the EU. It hones in on harmonising and making RIS interoperable across Member States, particularly on the trans-European transport network (TEN-T). It seeks to integrate inland waterway transport more seamlessly with other transport modes through digital solutions and data sharing, and establishes a European RIS Environment to streamline information access. The focus is on modernizing RIS to enhance digital integration and data accessibility.<\/p>\n<h5>Directive (EU) 2025\/2456<\/h5>\n<p>This directive streamlines the chemical safety assessment process by shifting responsibilities to the European Chemicals Agency (ECHA). The primary goal is to improve transparency, ease burdens on stakeholders, expedite decision-making, and ensure consistency in scientific evaluations. The directive aims to enhance the evaluation process for applications for exemptions from substance restrictions and the review of substances for potential restriction. It modernises the scientific assessment of chemicals to align with ECHA’s existing standards.<\/p>\n<h5>Commission Implementing Regulation (EU) 2025\/2540<\/h5>\n<p>This regulation establishes a detailed plan for peer review of national cybersecurity certification authorities (NCCAs). It aims to ensure consistent standards for European cybersecurity certificates by setting out a schedule, frequency, and methodology for peer reviews conducted by NCCAs from different Member States and the European Commission. Key elements include a rotation system for peer reviewers, criteria for team composition, guidelines for the review process, and requirements for the peer-review report. The objective is to build confidence in cybersecurity certifications across the EU by standardizing the assessment of NCCAs.<\/p>\n<h3><strong>Review of each of legal acts published today:<\/strong><\/h3>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2004\"><\/p>\n<h3><strong>Commission Delegated Regulation (EU) 2025\/2004 of 6\u00a0October 2025 amending Regulation (EU)\u00a02023\/2833 of the European Parliament and of the Council as regards derogations on reporting of intra-EU trade and certain tagging information, and the determination of weight of individual bluefin tuna<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This Commission Delegated Regulation (EU) 2025\/2004 amends Regulation (EU) 2023\/2833, which establishes a catch documentation program for bluefin tuna. The amendments address specific derogations on reporting intra-EU trade and certain tagging information, and they also change how the weight of individual bluefin tuna is determined. These changes are made in response to recommendations from the International Commission for the Conservation of Atlantic Tunas (ICCAT).<\/p>\n<p>The regulation consists of two articles. Article 1 outlines the specific amendments to Regulation (EU) 2023\/2833, replacing Article 5(4) regarding annual reporting by Member States on the implementation of derogations, requiring information on verification, outcomes, and trade data. It also replaces Article 6(5) concerning the determination of the approximate weight of individual fish, allowing Member States to use the average weight of the total landing weight divided by the number of fish, particularly for fisheries with minimum conservation reference size derogations. Article 2 stipulates that the regulation will enter into force on the day following its publication in the Official Journal of the European Union.<\/p>\n<p>The most important provisions for practical use are the changes to Article 5(4) and Article 6(5) of Regulation (EU) 2023\/2833. The amendment to Article 5(4) clarifies the reporting requirements for Member States regarding derogations on intra-EU trade, ensuring that the Commission receives comprehensive data on verification processes and trade activities. The amendment to Article 6(5) simplifies the process for determining the weight of individual bluefin tuna, aligning it with current practices where all landed fish are weighed, and sampling is unnecessary.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2002\"><\/p>\n<h3><strong>Commission Delegated Regulation (EU) 2025\/2002 of 6\u00a0October 2025 amending Regulation (EU)\u00a02017\/2107 of the European Parliament and of the Council as regards the number of fish aggregating devices permitted in the Convention area of the International Commission for the Conservation of Atlantic Tunas<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This Commission Delegated Regulation (EU) 2025\/2002 amends Regulation (EU) 2017\/2107, focusing on the management, conservation, and control measures within the Convention area of the International Commission for the Conservation of Atlantic Tunas (ICCAT). The key change introduced by this regulation is a reduction in the number of fish aggregating devices (FADs) allowed per vessel, aligning EU law with the latest ICCAT recommendation. This adjustment aims to further the long-term conservation and sustainable use of fishery resources in the Atlantic.<\/p>\n<p>The regulation consists of two articles. Article 1 directly amends Article 9(4) of Regulation (EU) 2017\/2107, stipulating that, starting from January 1, 2026, Member States must ensure that no more than 288 FADs per vessel with operational buoys are active at any given time. This is a decrease from the previously allowed number of 300 FADs. Article 2 states that the regulation will enter into force on the day following its publication in the Official Journal of the European Union, ensuring its swift implementation.<\/p>\n<p>The most important provision of this regulation is the amended limit on FADs per vessel, reducing it to 288. This change directly impacts Union fishing vessels operating in the ICCAT Convention area, requiring them to adjust their fishing practices and equipment deployment strategies to comply with the new limit by January 1, 2026.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2017\"><\/p>\n<h3><strong>Commission Delegated Regulation (EU) 2025\/2017 of 8\u00a0October 2025 amending Delegated Regulation (EU)\u00a02016\/127 as regards the protein-related requirements for infant and follow-on formula manufactured from protein hydrolysates<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This Commission Delegated Regulation (EU) 2025\/2017 amends Delegated Regulation (EU) 2016\/127, specifically concerning the protein-related requirements for infant and follow-on formula manufactured from protein hydrolysates. The amendment introduces an additional set of requirements, named “Protein-related requirements group E,” to the existing compositional requirements for protein hydrolysates. This addition is based on a favorable scientific opinion from the European Food Safety Authority (EFSA) regarding the safety and suitability of a specific protein hydrolysate manufactured by Fonterra Cooperative Group Ltd.<\/p>\n<p>The regulation modifies Annexes I, II, and III of Delegated Regulation (EU) 2016\/127. It replaces points 2.3 in both Annex I (for infant formula) and Annex II (for follow-on formula) with updated sections that include the new “Protein-related requirements group E,” alongside the existing groups A, B, C, and D. Each group specifies different requirements for protein content, protein source, protein processing, and indispensable and conditionally indispensable amino acids. Additionally, Annex III is updated to reflect the inclusion of the new protein-related requirements group.<\/p>\n<p>The main provision of this regulation is the introduction of “Protein-related requirements group E,” which sets specific criteria for infant and follow-on formula manufactured using the protein hydrolysate evaluated by EFSA. This includes minimum and maximum protein content (0,48-0,67 g\/100 kJ), a defined protein source (whey protein concentrate from cow’s milk with a minimum protein content of 80%), a specific protein processing method (two-stage hydrolysis with serine endopeptidases), and requirements for indispensable and conditionally indispensable amino acids. Manufacturers intending to use the Fonterra protein hydrolysate must adhere to these specific requirements to ensure their products comply with EU regulations.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025L2482\"><\/p>\n<h3><strong>Directive (EU) 2025\/2482 of the European Parliament and of the Council of 26 November 2025 amending Directive 2005\/44\/EC on harmonised river information services (RIS) on inland waterways in the Community<\/strong><\/h3>\n<p><\/a><\/p>\n<p>Okay, here’s a breakdown of Directive (EU) 2025\/2482, amending Directive 2005\/44\/EC on harmonised river information services (RIS) on inland waterways:<\/p>\n<p>**1. Essence of the Act:**<\/p>\n<p>This Directive updates the framework for River Information Services (RIS) to improve safety, efficiency, and sustainability of inland waterway transport within the EU. It focuses on enhancing the harmonisation and interoperability of RIS across Member States, particularly along the trans-European transport network (TEN-T). The directive aims to integrate inland waterway transport more seamlessly with other modes of transport through digital solutions and data sharing. It also establishes a European RIS Environment to streamline information access and exchange.<\/p>\n<p>**2. Structure and Main Provisions:**<\/p>\n<p>The Directive amends several articles of the original Directive 2005\/44\/EC and adds new provisions. Key changes include:<\/p>\n<p>* **Scope:** The application of the Directive is now primarily focused on inland waterways and ports that are part of the TEN-T and directly connected to another Member State’s TEN-T waterways.<br \/>\n* **Definitions:** New definitions are added for terms like “trans-European transport network,” “European Reference Data Management System,” “port community system,” “smart inland waterway infrastructure system,” “European RIS Environment,” and “inland port.”<br \/>\n* **Setting up RIS:** Member States are required to implement RIS on relevant waterways and ports, ensuring data is up-to-date and accessible. They must also enable electronic ship reporting and provide notices to skippers in standardised formats.<br \/>\n* **European RIS Environment:** A key element is the establishment of a European RIS Environment, a single-point-of-access platform for RIS information. Member States must jointly create, govern, and maintain this environment. The Commission is empowered to adopt implementing acts to define its operational characteristics.<br \/>\n* **Technical Specifications:** The Directive emphasizes the importance of technical specifications for RIS, covering areas like inland ECDIS, electronic ship reporting, and vessel tracking. It introduces the concept of referencing the European Standard for River Information Services (ES-RIS) developed by CESNI.<br \/>\n* **Feedback Mechanism:** A new article mandates Member States to have a procedure for handling feedback from RIS users, submitted through the European RIS Environment.<br \/>\n* **Data Protection:** The Directive includes provisions to ensure the protection of personal data processed for RIS operations, in accordance with EU data protection regulations.<br \/>\n* **Delegated Powers:** The Commission is granted powers to adopt delegated acts to amend Annex I (minimum data requirements) and Annex III (technical specifications), under certain conditions.<br \/>\n* **Committee Procedure:** The Inland Waterway Transport Committee will assist the Commission in matters related to RIS.<\/p>\n<p>**3. Main Provisions Important for Use:**<\/p>\n<p>* **Focus on TEN-T:** The restriction of the scope to the TEN-T network means that RIS implementation is prioritised on the most important waterways for EU transport policy.<br \/>\n* **European RIS Environment:** The establishment of the European RIS Environment as a central platform for information exchange is a key development for RIS users.<br \/>\n* **Technical Specifications and ES-RIS:** The reference to the European Standard for River Information Services (ES-RIS) ensures that RIS implementation is based on up-to-date and harmonised technical standards.<br \/>\n* **Feedback Mechanism:** The feedback mechanism provides a channel for RIS users to report issues and contribute to the improvement of RIS implementation.<br \/>\n* **Data Requirements:** The minimum data requirements outlined in Annex I are crucial for ensuring that RIS users have access to essential information for navigation and voyage planning.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025L2456\"><\/p>\n<h3><strong>Directive (EU) 2025\/2456 of the European Parliament and of the Council of 26 November 2025 amending Directive 2011\/65\/EU as regards the reattribution of scientific and technical tasks to the European Chemicals Agency (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><\/p>\n<p>Directive (EU) 2025\/2456 amends Directive 2011\/65\/EU, focusing on reallocating scientific and technical responsibilities to the European Chemicals Agency (ECHA) to streamline chemical safety assessments. The core aim is to enhance transparency, reduce burdens on stakeholders, accelerate decision-making, and ensure consistency in scientific evaluations. This involves expanding ECHA’s role in evaluating applications for exemptions from substance restrictions and in reviewing substances for potential inclusion in the list of restricted substances. The directive seeks to align processes with ECHA’s current standards, promote digitalization, and improve data accessibility and interoperability, ultimately leading to cost savings and efficiency gains.<\/p>\n<p>The Directive modifies Articles 5, 6, 20, and 24 of Directive 2011\/65\/EU and introduces Articles 6a, 6b, and 6c, along with a new Annex Va. Key changes include:<\/p>\n<p>* **Reattribution of Tasks to ECHA:** ECHA is now responsible for receiving and processing applications for exemptions, verifying their completeness, and making them available to Member States and the public.<br \/>\n* **Enhanced Review Process:** The directive introduces detailed procedural steps for reviewing substances for potential inclusion in the list of restricted substances, ensuring a more transparent and thorough assessment.<br \/>\n* **Committee Involvement:** The Committee for Socioeconomic Analysis and, where relevant, the Committee for Risk Assessment, will provide opinions on exemption applications and proposed restrictions.<br \/>\n* **Public Availability of Information:** ECHA will make summaries and non-confidential versions of applications, as well as parts of the committees’ opinions, publicly available on its website.<br \/>\n* **Periodic Review of Restricted Substances:** The list of restricted substances will be reviewed at least every four years.<br \/>\n* **Harmonized Formats and Guidelines:** ECHA will establish harmonized formats and comprehensive guidelines for applications, taking into account the situation of SMEs.<br \/>\n* **Restriction Dossiers:** The requirements for restriction dossiers are specified in the new Annex Va, ensuring that they contain all necessary information for a thorough assessment.<\/p>\n<p>The most important provisions for practical use are those related to the new roles and responsibilities of the European Chemicals Agency (ECHA) in the assessment of applications for exemptions and the review of restricted substances. Economic operators need to be aware of the harmonized formats and guidelines that ECHA will provide for submitting applications. Member States should take note of the new procedures for preparing and submitting restriction dossiers.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2540\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2540 of 9\u00a0December 2025 laying down rules for the application of Regulation (EU)\u00a02019\/881 of the European Parliament and of the Council as regards the establishment of the plan for peer review<\/strong><\/h3>\n<p><\/a><\/p>\n<p>This is a description of Commission Implementing Regulation (EU) 2025\/2540, which lays down rules for the application of Regulation (EU) 2019\/881 regarding the establishment of a plan for peer review of national cybersecurity certification authorities (NCCAs). The regulation aims to ensure equivalent standards for European cybersecurity certificates and EU statements of conformity by establishing a consistent peer review process across the Union. It outlines the schedule, frequency, and methodology for these peer reviews, involving NCCAs from different Member States and the European Commission. The regulation also addresses confidentiality, secure communication, and capacity-building aspects related to the peer review process.<\/p>\n<p>The regulation consists of 8 articles and 2 annexes.<\/p>\n<p>* **Article 1** establishes the schedule, frequency, and cost of peer reviews, with Annex I providing the specific schedule for each Member State. It allows for postponement requests in exceptional circumstances and clarifies the process for Member States with multiple NCCAs or those designating NCCAs from other Member States.<br \/>\n* **Article 2** sets up a rotation system for peer-reviewer NCCAs, ensuring that each NCCA participates in at least two peer reviews over a five-year period. It also allows for observer participation from other NCCAs and ENISA.<br \/>\n* **Article 3** outlines the criteria for the composition of the peer review team, including experience, knowledge, and independence requirements. It also establishes a process for addressing potential conflicts of interest.<br \/>\n* **Article 4** details the methodology for the peer review, including self-assessment questionnaires, documentation review, interviews, and on-site visits. It also addresses the language of cooperation and the responsibilities of the peer-reviewed NCCA.<br \/>\n* **Article 5** specifies the requirements for the peer-review report, including its content, timeline, and dissemination process. It also addresses the handling of comments from the peer-reviewed NCCA and the publication of a summary report.<br \/>\n* **Article 6** focuses on confidentiality, ensuring the protection of sensitive information obtained during the peer review process. It also mandates the deletion or destruction of documents after the final report is completed.<br \/>\n* **Article 7** tasks ENISA with analyzing the aggregated results of the peer reviews to identify lessons learned and best practices for capacity-building among NCCAs.<br \/>\n* **Article 8** states that the regulation will enter into force on the twentieth day following its publication in the Official Journal of the European Union.<br \/>\n* **Annex I** provides the schedule of NCCAs that are subject to peer review.<br \/>\n* **Annex II** describes the methodology of the peer review.<\/p>\n<p>The most important provisions for practical use are those concerning the schedule for peer reviews (Article 1 and Annex I), the criteria for peer review team composition (Article 3), the methodology for conducting the peer review (Article 4), and the requirements for the peer-review report (Article 5). These provisions provide a clear framework for NCCAs to prepare for and participate in the peer review process, ensuring a consistent and effective assessment of their cybersecurity certification activities.<\/p>\n<p><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2513\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2513 of 11\u00a0December 2025 concerning the authorisation of copper(II)-betaine complex as a feed additive for all animal species<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2501\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2501 of 11\u00a0December 2025 amending Implementing Regulation (EU)\u00a02021\/1165 as regards the use of certain products and substances in organic production<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2503\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2503 of 11\u00a0December 2025 concerning the authorisation of a preparation of endo-1,4-beta-xylanase, endo-1,4-beta-glucanase and xyloglucan-specific-endo-beta-1,4-glucanase produced with Trichoderma citrinoviride DSM 33578 as a feed additive for poultry other than poultry for fattening, poultry reared for laying and reared for breeding and porcine species other than sows of all Suidae species (holder of authorisation: Huvepharma EOOD)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2502\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2502 of 11\u00a0December 2025 concerning the authorisation of a preparation of protease produced with Bacillus subtilis CBS 148232 and viable spores of Bacillus velezensis NRRL B-50508, Bacillus velezensis NRRL B-50509 and Bacillus subtilis NRRL B-50510 as a feed additive for pigs for fattening of all Suidae species and weaned piglets of minor Suidae species (holder of authorisation: Genencor International B.V.)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2505\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2505 of 11\u00a0December 2025 concerning the authorisation of guanidinoacetic acid and a preparation of guanidinoacetic acid as feed additives for weaned piglets and pigs for fattening in water for drinking and for turkeys for fattening and reared for breeding in feed and water for drinking (holder of authorisation: Alzchem Trostberg GmbH), and amending Implementing Regulation (EU)\u00a02023\/2628<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2500\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2500 of 11\u00a0December 2025 concerning the authorisation of a preparation of Bacillus velezensis NRRL B-67647, Bacillus pumilus NRRL B-67648 and Bacillus licheniformis NRRL B-67649 as a feed additive for poultry for fattening and ornamental birds (holder of authorisation: S.I.Lesaffre)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2543\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2543 of 11\u00a0December 2025 concerning the denial of the renewal of the authorisation of Patent Blue V as a feed additive for non-food producing animals and repealing Implementing Regulation (EU) No\u00a0643\/2013<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2511\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2511 of 11\u00a0December 2025 concerning the authorisation of a preparation of Bacillus paralicheniformis DSM 33902 and Bacillus subtilis DSM 33903 as a feed additive for ruminants for milk production\/reproduction (holder of authorisation: Chr. Hansen\u00a0A\/S)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2498\"><\/p>\n<h3><strong>Commission Implementing Regulation (EU) 2025\/2498 of 11\u00a0December 2025 concerning the authorisation of 4-hydroxy-2,5-dimethylfuran-3(2H)-one as a feed additive for all animal species, except cats and dogs<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2457\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2457 of the European Parliament and of the Council of 26 November 2025 amending Regulations (EC) No 178\/2002, (EC) No 401\/2009, (EU) 2017\/745 and (EU) 2019\/1021 as regards the reattribution of scientific and technical tasks and improving cooperation among Union agencies in the area of chemicals (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2458\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2458 of the European Parliament and of the Council of 26 November 2025 on European statistics on population and housing, amending Regulation (EC) No 862\/2007 and repealing Regulations (EC) No 763\/2008 and (EU) No 1260\/2013 (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2518\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2518 of the European Parliament and of the Council of 26 November 2025 laying down additional procedural rules on the enforcement of Regulation (EU) 2016\/679 (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2509\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2509 of the European Parliament and of the Council of 26 November 2025 on the safety of toys and repealing Directive 2009\/48\/EC (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><br \/>\n<a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/AUTO\/?uri=CELEX:32025R2455\"><\/p>\n<h3><strong>Regulation (EU) 2025\/2455 of the European Parliament and of the Council of 26 November 2025 establishing a common data platform on chemicals, laying down rules to ensure that the data contained in it are findable, accessible, interoperable and reusable and establishing a monitoring and outlook framework for chemicals (Text with EEA relevance)<\/strong><\/h3>\n<p><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>EU Legal Acts Review Review of EU Legal Acts Commission Delegated Regulation (EU) 2025\/2004 This regulation modifies existing rules on bluefin tuna catch documentation. Key changes include simplified reporting requirements for Member States regarding derogations on intra-EU trade, making it easier for the Commission to track trade verification and outcomes. Additionally, it streamlines the process…<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_bbp_topic_count":0,"_bbp_reply_count":0,"_bbp_total_topic_count":0,"_bbp_total_reply_count":0,"_bbp_voice_count":0,"_bbp_anonymous_reply_count":0,"_bbp_topic_count_hidden":0,"_bbp_reply_count_hidden":0,"_bbp_forum_subforum_count":0,"pmpro_default_level":"","footnotes":""},"categories":[14],"tags":[],"class_list":["post-13913","post","type-post","status-publish","format-standard","hentry","category-eu-legislation-detailed","pmpro-has-access"],"acf":{"patreon-level":0},"_links":{"self":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/posts\/13913","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/comments?post=13913"}],"version-history":[{"count":0,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/posts\/13913\/revisions"}],"wp:attachment":[{"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/media?parent=13913"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/categories?post=13913"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lexcovery.com\/en\/wp-json\/wp\/v2\/tags?post=13913"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}