Commission Implementing Regulation (EU) 2025/1419
This regulation simply updates the name of a company, Zoetis Belgium S.A., to Phibro Animal Health SA, in several existing regulations related to feed additives. A transitional period is provided for products labelled with the old name.
Commission Implementing Regulation (EU) 2025/1420
This regulation lays down the rules for application of the Interoperable Europe Act. It establishes and operates interoperability regulatory sandboxes. Sandboxes are established through specific agreements between at least three Union entities or public sector bodies and requires notification and authorization of the sandbox by the Commission through the Interoperable Europe Portal.
It defines rights and obligations of coordinators and participants, and it emphasizes risk management and data protection.
Commission Implementing Regulation (EU) 2025/1424
This regulation renews the authorization for biotin as a feed additive for all animal species. It details the specific conditions for its use and allows for the continued use of products produced under the previous regulation for a limited time.
Commission Implementing Regulation (EU) 2025/1422
This regulation amends the list of invasive alien species of Union concern. It adds new species, updates nomenclature, and clarifies the scope of certain species. This triggers restrictions on their import, keeping, breeding, transport, and release into the environment.
Commission Implementing Regulation (EU) 2025/1462
This regulation registers ‘Kőszeg / Kőszegi’ as a Protected Designation of Origin (PDO) in the EU, meaning only products from that region meeting specific standards can use the name.
Commission Implementing Regulation (EU) 2025/1456
This regulation imposes a provisional anti-dumping duty on imports of fused alumina from China. It defines the product, details how dumping was determined and the injury to the Union industry, and specifies duty rates for different companies.
Commission Implementing Regulation (EU) 2025/1426
This regulation authorizes the use of a specific preparation of *Saccharomyces cerevisiae* as a feed additive for several animal categories and amends previous regulations for its use in lambs, including conditions and transitional measures.
Commission Implementing Regulation (EU) 2025/1423
This regulation amends the authorization for a canthaxanthin preparation used as a feed additive for breeder hens. It introduces a new production method, modifies additive specifications, and increases the limit for dichloromethane impurity.
Commission Implementing Regulation (EU) 2025/1510
This regulation updates lists of regions in Canada and the United States from which the entry of poultry products into the EU is authorized or suspended due to outbreaks of avian influenza.
Commission Implementing Regulation (EU) 2025/1418
This regulation renews the authorization for a specific feed additive, a preparation of enzymes, for poultry and pigs. It sets out conditions for use and repeals previous regulations.
Commission Implementing Regulation (EU) 2025/1427
This regulation introduces the registration of imports of certain polyethylene terephthalate (PET) originating in Vietnam, which means that it opens the door for potential retroactive anti-dumping duties.
Commission Implementing Regulation (EU) 2025/1417
This regulation authorizes the use of Spanish type origanum essential oil as a sensory feed additive (flavouring compound) for all animal species, setting conditions for use, including maximum content levels, labelling requirements, and user protection measures.
Commission Implementing Regulation (EU) 2025/1325
This regulation amends standard forms and computerised formats for the automatic exchange of information under Directive 2011/16/EU, ensuring a standardised XML schema for reporting financial and tax-related information of multinational enterprises.
Commission Implementing Regulation (EU) 2025/1400
This regulation authorises the use of peppermint, clary sage, and sage essential oils as sensory feed additives (flavouring compounds) for all animal species, setting maximum content levels and specifying labelling requirements and user protection measures.
Commission Implementing Regulation (EU) 2025/1402
This regulation authorises the use of tea tree essential oil as a sensory feed additive for all animal species, setting conditions for its use, including maximum content levels in feed and protective measures for users.
Commission Implementing Regulation (EU) 2025/1403
This regulation authorises the use of Spanish sage and lavender essential oils as sensory feed additives, defining conditions for use, maximum content levels, and labelling requirements, along with transitional measures for existing products.
Decision of the EU-Canada Joint Customs Cooperation Committee
This decision establishes mutual recognition between the EU’s Authorised Economic Operator (AEO) programme and Canada’s Partners in Protection (PIP) programme to facilitate trade and enhance security. It outlines how customs authorities will cooperate and exchange information.
Review of each of legal acts published today:
Commission Implementing Regulation (EU) 2025/1419 of 17 July 2025 amending Implementing Regulations (EU) 2020/148, (EU) 2021/2094 and (EU) 2023/1172 as regards the name of the holder of the authorisation for feed additives
This Commission Implementing Regulation (EU) 2025/1419 amends Implementing Regulations (EU) 2020/148, (EU) 2021/2094, and (EU) 2023/1172 to reflect a change in the name of the company holding the authorization for certain feed additives. Specifically, the name of the authorization holder is changed from Zoetis Belgium S.A. to Phibro Animal Health SA. The regulation ensures that the marketing rights are correctly attributed to the new name of the company.
The structure of the act is straightforward. It consists of 5 articles. Articles 1, 2, and 3 directly amend the titles and relevant sections of the annexes of Implementing Regulations (EU) 2020/148, (EU) 2021/2094, and (EU) 2023/1172, respectively, by replacing the previous company name with the new one. Article 4 provides a transitional measure allowing existing stocks produced and labelled with the old name to be sold and used until they are exhausted. Article 5 specifies that the regulation will enter into force twenty days after its publication in the Official Journal of the European Union.
The most important provision for practical use is Article 4, the transitional measure. This allows businesses to continue using and selling existing stocks of the feed additives that were produced and labelled under the previous company name (Zoetis Belgium S.A.) without needing to immediately relabel or discard them. This provides flexibility and avoids potential economic losses for businesses holding these stocks.
Commission Implementing Regulation (EU) 2025/1420 of 17 July 2025 laying down rules for the application of Regulation (EU) 2024/903 of the European Parliament and of the Council, as regards the establishment and the operation of the interoperability regulatory sandboxes
This is a description of the **Commission Implementing Regulation (EU) 2025/1420** of 17 July 2025, which lays down rules for the application of Regulation (EU) 2024/903, also known as the Interoperable Europe Act, concerning the establishment and operation of interoperability regulatory sandboxes. This regulation provides detailed guidelines and procedures for setting up and managing these sandboxes, which are designed to foster innovation and cross-border interoperability of digital public services within the EU. The regulation aims to ensure that these sandboxes operate effectively, transparently, and in compliance with relevant EU laws, including data protection regulations.
**Structure and Main Provisions:**
The regulation is structured into four chapters, covering general provisions, the establishment of interoperability regulatory sandboxes, their operation, and final provisions.
* **Chapter I (General Provisions):** Defines key terms such as “project,” “regulatory sandbox coordinators,” “specific agreement,” “regulator,” and “specific plan” to ensure a common understanding of the regulation’s scope.
* **Chapter II (Establishment of an Interoperability Regulatory Sandbox):**
* Specifies that a sandbox must be established through a specific agreement between at least three Union entities or public sector bodies.
* Outlines the criteria for establishing a sandbox, including contributing to the objectives of the Interoperable Europe Act, assessing the possibility of joining existing sandboxes, and concluding a specific agreement with essential elements like objectives, governance, risk management, and evaluation frameworks.
* Requires notification and authorization of the sandbox by the Commission through the Interoperable Europe Portal.
* Ensures transparency by requiring the Commission to create a dedicated interface for information and exchange on interoperability regulatory sandboxes within the Interoperable Europe Portal.
* Sets conditions for the renewal or closing of a sandbox.
* **Chapter III (Operation of Interoperability Regulatory Sandboxes):**
* Defines the general rights and obligations of regulatory sandbox coordinators, including inviting regulators, steering regulatory dialogue, selecting projects, ensuring participation is based on a specific plan, and setting up a risk management framework.
* Specifies the process for admitting participants and other actors, such as GovTech entities, to the sandbox.
* Outlines the general rights and obligations of participants, including contributing to the specific plan, assuming responsibility for the legality of their activities, complying with data protection laws, and adhering to the risk management framework.
* Details the risk management process, including the establishment of a risk management plan for each project and the appointment of a risk manager.
* Establishes reporting obligations, including periodic reports to the Commission and the Interoperable Europe Board.
* Sets conditions for participants exiting the sandbox and the termination of a project.
* **Chapter IV (Final Provisions):** Specifies the date of entry into force of the regulation.
**Main Provisions for Practical Use:**
* **Establishment Criteria (Article 3):** Public sector bodies and Union entities need to meet specific criteria, including contributing to the objectives of the Interoperable Europe Act and concluding a detailed specific agreement.
* **Notification and Authorisation (Article 5):** A joint request must be sent through the Interoperable Europe Portal, including all necessary information for the Commission to assess compliance.
* **Transparency (Article 6):** The Commission will maintain a dedicated interface on the Interoperable Europe Portal for information and exchange on interoperability regulatory sandboxes.
* **Rights and Obligations of Coordinators and Participants (Articles 9 & 11):** These articles clearly define the responsibilities of those managing and participating in the sandboxes, ensuring accountability and compliance.
* **Risk Management (Article 12):** A detailed risk management process must be established, including a specific risk management plan for each project and the appointment of a risk manager.
* **Reporting Obligations (Article 13):** Regular reporting to the Commission and the Interoperable Europe Board is required, covering progress, outcomes, and challenges.
* **Data Protection (Articles 3, 9, 11 & Annex):** The regulation emphasizes compliance with data protection laws, particularly when processing personal data, ensuring the involvement of data protection authorities.
Commission Implementing Regulation (EU) 2025/1424 of 17 July 2025 concerning the renewal of the authorisation of biotin and two preparations of biotin as feed additives for all animal species and repealing Implementing Regulation (EU) 2015/723
This Commission Implementing Regulation (EU) 2025/1424 concerns the renewal of the authorization for biotin and two biotin preparations as feed additives for all animal species. It also repeals the previous regulation, Implementing Regulation (EU) 2015/723, which initially authorized biotin.
The regulation is structured as follows: It consists of a preamble that outlines the reasons and justifications for the renewal, followed by four articles and an annex. Article 1 renews the authorization of biotin and its preparations, specifying that they belong to the category of nutritional additives. Article 2 repeals Implementing Regulation (EU) 2015/723. Article 3 outlines transitional measures for products already on the market. Article 4 states the regulation’s entry into force. The Annex provides detailed information on the authorized additives, including their composition, identification number, and specific conditions of use.
The most important provisions for practical use are found in the Annex, which details the specific conditions for the use of biotin and its preparations. These include the composition, analytical methods, and other provisions such as the requirement for feed business operators to establish operational procedures and organizational measures to address potential risks to users of the additive, including the use of personal breathing protective equipment where risks cannot be eliminated. The transitional measures in Article 3 are also important, as they allow for the continued use of products produced and labeled under the previous regulation for a limited time, ensuring a smooth transition to the new requirements.
Commission Implementing Regulation (EU) 2025/1422 of 17 July 2025 amending Implementing Regulation (EU) 2016/1141 to update the list of invasive alien species of Union concern
This is Commission Implementing Regulation (EU) 2025/1422 amending Implementing Regulation (EU) 2016/1141 to update the list of invasive alien species of Union concern. The Regulation updates the list of invasive alien species of Union concern based on risk assessments and available evidence, in accordance with Regulation (EU) No 1143/2014. It adds new species to the list, updates the nomenclature of existing species, and clarifies the scope of certain species already listed.
The structure of the act is straightforward. It consists of two articles and an annex. Article 1 states that the Annex to Implementing Regulation (EU) 2016/1141 is amended in accordance with the Annex to this Regulation. Article 2 specifies the date of entry into force and a specific date of application for one of the points in the Annex. The Annex provides detailed amendments to the table in the Annex to Implementing Regulation (EU) 2016/1141, including adding new species, updating nomenclature, and adding notes for clarification.
The most important provisions for practical use are those that directly impact the obligations of Member States and individuals regarding invasive alien species. These include the addition of new species to the Union list, which triggers restrictions on their import, keeping, breeding, transport, and release into the environment. The changes to the nomenclature of existing species and the clarification of the scope of Lampropeltis getula are also important to ensure that the correct species are targeted by the regulations. The deferred application for Castor canadensis and Neogale vison provides a temporary reprieve for Member States to prepare for the management of these species.
Commission Implementing Regulation (EU) 2025/1462 of 11 July 2025 on the registration of the geographical indication Kőszeg / Kőszegi (PDO) in the Union register of geographical indications pursuant to Regulation (EU) 2024/1143 of the European Parliament and of the Council
This Commission Implementing Regulation (EU) 2025/1462 registers the geographical indication ‘Kőszeg / Kőszegi’ as a Protected Designation of Origin (PDO) in the Union register. This registration is based on an application from Hungary and follows the procedures outlined in Regulation (EU) 2024/1143, which governs geographical indications for various agricultural products. Since no objections were received, the geographical indication is now officially protected at the EU level.
The regulation consists of a preamble that cites the relevant legal bases and justifications for the decision, followed by two articles. Article 1 formally registers the geographical indication ‘Kőszeg / Kőszegi’ (PDO) in the Union register, as per Article 22 of Regulation (EU) 2024/1143. Article 2 specifies that the regulation will come into force twenty days after its publication in the Official Journal of the European Union, making it binding and directly applicable in all Member States. This regulation implements the provisions of Regulation (EU) 2024/1143, which repealed Regulation (EU) No 1151/2012, and builds upon previous regulations such as Regulation (EU) No 1308/2013.
The most important provision is Article 1, which grants legal protection to the name ‘Kőszeg / Kőszegi’ as a PDO within the EU. This means that only products originating from the specified geographical area and meeting specific production standards can be marketed under that name, preventing misuse and ensuring consumers can trust the origin and quality of the product.
Commission Implementing Regulation (EU) 2025/1456 of 17 July 2025 imposing a provisional anti-dumping duty on imports of fused alumina originating in the People’s Republic of China
Here’s a breakdown of the Commission Implementing Regulation (EU) 2025/1456, focusing on its key aspects:
**1. Essence of the Act:**
This regulation imposes a provisional anti-dumping duty on imports of fused alumina originating from the People’s Republic of China (PRC). The European Commission initiated this action following an investigation that found evidence of dumping (selling products at unfairly low prices) by Chinese producers, which was causing material injury to the Union industry. The regulation aims to counteract these unfair trade practices by applying duties to level the playing field.
**2. Structure and Main Provisions:**
* **Initiation and Investigation:** The regulation details the process of initiating the anti-dumping investigation, including the complaint, registration of imports, and involvement of interested parties.
* **Product Definition:** It clearly defines the “product under investigation” (fused alumina) and the “like product” produced by the Union industry. It also addresses claims regarding the product scope, specifically whether certain types of corundum should be excluded.
* **Dumping Determination:** A significant portion of the regulation explains how the Commission determined that dumping was taking place. Due to significant distortions in the Chinese economy, the normal value (price in the exporting country) was constructed based on costs in a representative country (Brazil). The export price was then compared to this constructed normal value to calculate dumping margins.
* **Injury Assessment:** The regulation assesses the injury suffered by the Union industry due to the dumped imports, considering factors like production, sales, market share, and profitability.
* **Causation Analysis:** It examines the causal link between the dumped imports and the injury to the Union industry, while also considering other potential factors that could have contributed to the injury.
* **Level of Measures:** The regulation determines the level of anti-dumping duties needed to remove the injury to the Union industry.
* **Union Interest:** It assesses whether imposing anti-dumping measures is in the overall interest of the European Union, considering the interests of the Union industry, importers, and users.
* **Provisional Measures:** Based on its findings, the regulation imposes provisional anti-dumping duties on imports of fused alumina from the PRC.
* **Registration:** The regulation discontinues the registration of imports.
**3. Main Provisions Most Important for Use:**
* **Article 1:** This article is the core of the regulation. It clearly defines the product subject to the duty, specifies the duty rates for individual companies and all other imports from the PRC, and outlines the conditions for applying individual duty rates (presentation of a valid commercial invoice).
* **Duty Rates:** The specific anti-dumping duty rates listed in Article 1 are crucial for importers and exporters to determine the financial impact of the regulation on their trade.
* **Product Scope:** The definition of the product under investigation is important to determine whether specific products are subject to the duty.
* **Article 2:** This article specifies the deadlines for interested parties to submit comments or request hearings, which is important for those who wish to influence the final decision.
Commission Implementing Regulation (EU) 2025/1426 of 17 July 2025 concerning the authorisation of a preparation of Saccharomyces cerevisiae CNCM I-1077 as a feed additive for ruminants (other than lambs) and camelids reared for milk production or reared for reproduction, young ruminants for fattening other than calves and lambs, camelid calves for fattening, and Equidae other than horses (holder of authorisation: Lallemand SAS) and amending Implementing Regulation (EU) 2020/149 as regards the terms of the authorisation of a preparation of Saccharomyces cerevisiae CNCM I-1077 as a feed additive for lambs
This Commission Implementing Regulation (EU) 2025/1426 authorises the use of a specific preparation of *Saccharomyces cerevisiae* CNCM I-1077 as a feed additive for several animal categories. It also amends Implementing Regulation (EU) 2020/149 to modify the terms of authorisation for the same additive when used for lambs.
The Regulation consists of four articles and an annex. Article 1 authorises the *Saccharomyces cerevisiae* preparation as a feed additive under specific conditions. Article 2 amends Implementing Regulation (EU) 2020/149, reducing the minimum inclusion level of the additive in feed for lambs. Article 3 provides transitional measures, allowing the continued use of existing stocks of the additive and related products produced and labelled under the previous regulations for a limited time. Article 4 states that the regulation will come into force twenty days after its publication in the Official Journal of the European Union. The Annex specifies the conditions of use, including the animal species, minimum and maximum content, and other provisions. Compared to previous regulations, this act expands the use of the additive to additional animal categories and adjusts the minimum content for lambs.
The most important provisions of this act are those specifying the conditions of use for the *Saccharomyces cerevisiae* CNCM I-1077 preparation, as detailed in the Annex. These include the specific animal categories for which the additive is authorised (ruminants other than lambs, camelids, young ruminants for fattening other than calves and lambs, camelid calves for fattening, and Equidae other than horses), the minimum content of the additive in feed, and the requirement for feed business operators to establish operational procedures and organisational measures to address potential risks to users of the additive.
Commission Implementing Regulation (EU) 2025/1423 of 17 July 2025 amending Implementing Regulation (EU) No 684/2014 as regards the terms of the authorisation of a preparation of canthaxanthin as a feed additive for breeder hens (holder of authorisation: DSM Nutritional Products Ltd.)
This Commission Implementing Regulation (EU) 2025/1423 amends Implementing Regulation (EU) No 684/2014 regarding the authorization terms for a canthaxanthin preparation used as a feed additive for breeder hens. The amendment introduces a new production method using fermentation with Yarrowia lipolytica CBS 146148, modifies additive specifications by replacing ethoxyquin with butylated hydroxytoluene, and increases the limit for dichloromethane impurity. The regulation updates the Annex to Implementing Regulation (EU) No 684/2014 with these changes and includes transitional measures for products already on the market.
The regulation consists of three articles and an annex. Article 1 replaces the Annex to Implementing Regulation (EU) No 684/2014 with a new Annex, detailing the updated terms of authorization for canthaxanthin. Article 2 outlines transitional measures, allowing the continued use and marketing of products produced and labeled before specific dates under the previous regulations. Article 3 states that the regulation will enter into force twenty days after its publication in the Official Journal of the European Union. The Annex specifies the additive composition, including the new production method, chemical formula, description, analytical methods, and conditions of use for breeder hens. It sets maximum content levels, other provisions, and maximum residue limits in animal products.
The most important provisions for users include the updated additive composition, which now includes canthaxanthin produced by fermentation with Yarrowia lipolytica CBS 146148 and specifies the use of butylated hydroxytoluene instead of ethoxyquin. The increased limit for dichloromethane impurity (≤ 80 mg/kg additive) is also significant. Additionally, the transitional measures in Article 2 are crucial for businesses to manage their existing stock and adapt to the new requirements. The updated Annex also includes specific instructions for the use of the additive and premixture, including storage conditions, heat treatment, and the mixing of different sources and types of carotenoids.
Commission Implementing Regulation (EU) 2025/1510 of 17 July 2025 amending Annexes V and XIV to Implementing Regulation (EU) 2021/404 as regards the entries for Canada and the United States in the lists of third countries, territories or zones thereof authorised for the entry into the Union of consignments of poultry and germinal products of poultry and of fresh meat of poultry
This Commission Implementing Regulation (EU) 2025/1510 amends Annexes V and XIV to Implementing Regulation (EU) 2021/404, specifically concerning the entries for Canada and the United States in the lists of third countries, territories, or zones authorized for the entry into the Union of consignments of poultry, germinal products of poultry, and fresh meat of poultry.
The Regulation updates the lists of regions in Canada and the United States from which the entry of poultry products into the EU is authorized or suspended due to outbreaks of highly pathogenic avian influenza (HPAI). It re-authorizes the entry of poultry products from certain zones in Canada and the United States following the implementation of stamping-out policies and completion of cleaning and disinfection. At the same time, it suspends the entry of such products from a newly affected zone in the United States (Pennsylvania) due to a recent HPAI outbreak.
The main provisions of the act are the amendments to Annex V and XIV of Implementing Regulation (EU) 2021/404. These amendments consist of replacing existing rows and adding new rows for specific zones within Canada and the United States. Each row specifies the country, the zone code, the categories of poultry and products allowed (or suspended), the applicable restrictions (N, P1), the date of the outbreak, and the end date of the restriction (if applicable). The regulation enters into force on the day following its publication in the Official Journal of the European Union, ensuring its swift implementation.
Commission Implementing Regulation (EU) 2025/1418 of 17 July 2025 concerning the renewal of the authorisation of a preparation of endo-1,3(4)-beta-glucan’s and endo-1,4-beta-xylanase produced with Talaromyces versatilis IMI CC 378536 as a feed additive for all poultry species, weaned piglets, pigs for fattening and sows (holder of authorisation: Adisseo France S.A.S.) and repealing Implementing Regulations (EU) No 290/2014 and (EU) No 1138/2014
This Commission Implementing Regulation (EU) 2025/1418 concerns the renewal of the authorization for a feed additive used in animal nutrition. The additive is a preparation of endo-1,3(4)-beta-glucanase and endo-1,4-beta-xylanase produced with Talaromyces versatilis IMI CC 378536. The regulation extends the use of this additive for all poultry species, weaned piglets, pigs for fattening, and sows. It also repeals previous regulations (EU) No 290/2014 and (EU) No 1138/2014 that initially authorized the additive.
The regulation consists of three articles and an annex. Article 1 renews the authorization of the feed additive, classifying it as a ‘zootechnical additive’ with the functional group ‘digestibility enhancers,’ subject to the conditions outlined in the annex. Article 2 repeals the previous regulations that initially authorized the additive. Article 3 states that the regulation will come into force twenty days after its publication in the Official Journal of the European Union. The annex specifies details such as the additive’s composition, analytical methods, animal species for which it is intended, and other provisions, including storage conditions, heat treatment, and safety measures for users.
The most important provisions for users include the extended authorization for all poultry species, weaned piglets, pigs for fattening, and sows, as well as the specific conditions for use outlined in the annex. These conditions include the required storage conditions, heat treatment instructions, and safety measures to protect users from potential health risks, such as respiratory and dermal sensitization.
Commission Implementing Regulation (EU) 2025/1427 of 17 July 2025 making imports of certain polyethylene terephthalate (PET) originating in Vietnam subject to registration
This Commission Implementing Regulation (EU) 2025/1427 introduces the registration of imports of certain polyethylene terephthalate (PET) originating in Vietnam. This action is a preliminary step that allows the European Commission to potentially impose anti-dumping duties retroactively if the ongoing investigation confirms that these imports are being dumped and are causing injury to the Union industry. The registration of imports will enable the collection of duties from the date of registration, should the investigation lead to the imposition of definitive anti-dumping duties.
The regulation consists of a preamble outlining the reasons for the registration and two articles. The preamble refers to the initiation of an anti-dumping proceeding regarding PET imports from Vietnam, based on a complaint by PET Europe. It specifies that the product subject to registration is polyethylene terephthalate with a viscosity of 78 ml/g or higher, classified under CN code 3907 61 00. The regulation clarifies that the decision to register imports is based on Article 14(5) of the basic Regulation (EU) 2016/1036, which allows for such measures to ensure the possible retroactive application of anti-dumping duties. It also addresses the processing of personal data collected during the registration process, ensuring compliance with Regulation (EU) 2018/1725. Article 1 directs customs authorities to register imports of the specified PET originating in Vietnam, and specifies that the registration will expire nine months after the regulation’s entry into force. Article 2 states that the regulation will enter into force on the day following its publication in the Official Journal of the European Union.
The most important provision of this act is Article 1, which mandates the registration of specific PET imports from Vietnam. This means that importers of the product described in the regulation must ensure that their imports are properly recorded by the customs authorities. This registration is crucial because it opens the door for potential retroactive anti-dumping duties, which could significantly impact the financial implications of these imports. The nine-month expiration period for the registration is also a key element, as it sets a time frame for the investigation and any subsequent decisions on definitive duties.
Commission Implementing Regulation (EU) 2025/1417 of 17 July 2025 concerning the authorisation of Spanish type origanum essential oil from Thymbra capitata (L.) Cav. as a feed additive for all animal species
This Commission Implementing Regulation (EU) 2025/1417 authorises the use of Spanish type origanum essential oil from Thymbra capitata (L.) Cav. as a sensory feed additive (flavouring compound) for all animal species. It specifies the conditions of use, including maximum content levels in feed, and labelling requirements to ensure safe and effective application. The regulation also addresses the protection of users from potential health risks associated with the additive.
The regulation consists of three articles and an annex. Article 1 authorises the use of the additive under the conditions specified in the annex. Article 2 provides transitional measures for products already on the market. Article 3 states that the regulation will enter into force twenty days after its publication in the Official Journal of the European Union. The Annex specifies the identification number of the feed additive, its composition, analytical method, the animal species for which it is intended, and other provisions, including labelling requirements and user safety measures. Compared to previous authorisations under Directive 70/524/EEC, this regulation provides more specific conditions of use, including recommended maximum content levels for different animal species and categories, and mandates specific labelling requirements to ensure user safety.
Key provisions include the authorisation of Spanish type origanum essential oil as a feed additive for all animal species, with specific maximum content levels depending on the animal species. The regulation mandates that the additive be incorporated into feed as a premixture and specifies storage conditions and heat treatment stability in the directions for use. It also requires specific labelling information, including the recommended maximum content of the active substance, and imposes obligations on feed business operators to establish operational procedures and organisational measures to address potential risks to users, including the use of personal protective equipment where risks cannot be eliminated.
Commission Implementing Regulation (EU) 2025/1325 of 7 July 2025 amending Implementing Regulation (EU) 2015/2378 as regards the standard forms and computerised formats to be used for the mandatory automatic exchange of information under Council Directive 2011/16/EU as amended by Council Directive (EU) 2025/872
This is a description of the **Commission Implementing Regulation (EU) 2025/1325**.
**Essence of the Act:**
The regulation amends Implementing Regulation (EU) 2015/2378 to update the standard forms and computerised formats used for the automatic exchange of information under Council Directive 2011/16/EU, as amended by Council Directive (EU) 2025/872. These changes are necessary to facilitate the reporting and exchange of information related to multinational enterprise groups and large-scale domestic groups, as required by Directive 2011/16/EU. The regulation ensures that the automatic exchange of information is carried out using a standardised computerised format, as detailed in Annex XVII.
**Structure and Main Provisions:**
The regulation consists of two articles and an annex.
* **Article 1** amends Implementing Regulation (EU) 2015/2378 by adding a new paragraph to Article 2, specifying that the computerised format for the automatic exchange of information under Article 8ae(5) of Directive 2011/16/EU must comply with Annex XVII of the regulation. It also adds Annex XVII to Implementing Regulation (EU) 2015/2378.
* **Article 2** states that the regulation will come into force twenty days after its publication in the Official Journal of the European Union and that it is binding in its entirety and directly applicable in all Member States.
* **Annex XVII** provides the detailed computerised format (XML schema) to be used for the mandatory automatic exchange of information, including various data types, enumerations, and complex types for reporting financial and tax-related information of multinational enterprises.
**Main Provisions for Use:**
The most important provision for use is Annex XVII, which provides the technical specifications for the computerised format that must be used for the automatic exchange of information. This includes:
* Detailed XML schema definitions for various reporting elements.
* Specific enumerations (MessageType\_EnumType, MessageTypeIndic\_EnumType, IDTypeRules\_EnumType, etc.) that define the allowed values for certain data fields.
* Complex types (MessageSpec\_Type, TIN\_Type, GLOBEBody\_Type, etc.) that specify the structure and content of the data to be exchanged.
* Requirements for reporting various aspects of the GloBE (Global Anti-Base Erosion) rules, including corporate structure, financial data, tax computations, and jurisdictional information.
Commission Implementing Regulation (EU) 2025/1400 of 16 July 2025 concerning the authorisation of peppermint essential oil from Mentha × piperita L., clary sage essential oil from Salvia sclarea L. and sage essential oil from Salvia officinalis L. as feed additives for all animal species
This Commission Implementing Regulation (EU) 2025/1400 authorises the use of peppermint essential oil from Mentha × piperita L., clary sage essential oil from Salvia sclarea L., and sage essential oil from Salvia officinalis L. as sensory feed additives (flavouring compounds) for all animal species. It sets out specific conditions for their use, including maximum content levels in complete feed, labeling requirements, and necessary protective measures for users of these additives. The regulation aims to ensure the safety and efficacy of these substances in animal nutrition.
The regulation consists of three articles and an annex. Article 1 outlines the authorisation of the specified substances as feed additives under the category of sensory additives and the functional group of flavouring compounds, subject to the conditions detailed in the annex. Article 2 establishes transitional measures, allowing for the continued marketing and use of products produced and labeled before specific dates, in accordance with previous regulations, until existing stocks are exhausted. Article 3 states that the regulation will come into force twenty days after its publication in the Official Journal of the European Union. The Annex specifies for each of the three additives: the composition, description, analytical method, the animal species for which it is intended, the maximum content, other provisions and the end of the period of authorisation.
The most important provisions of this act are those laid down in the Annex. It specifies the maximum content of each additive per kilogram of complete feedingstuff, which varies depending on the animal species. It also mandates that the additives be incorporated into feed in the form of a premixture and outlines specific labeling requirements for both the additives and premixtures. Furthermore, it emphasizes the need for feed business operators to establish operational procedures and organisational measures to address potential risks to users, including the use of personal protective equipment where risks cannot be eliminated otherwise.
Commission Implementing Regulation (EU) 2025/1402 of 16 July 2025 concerning the authorisation of tea tree essential oil from Melaleuca alternifolia (Maiden & Betche) Cheel as a feed additive for all animal species
This Commission Implementing Regulation (EU) 2025/1402 authorises the use of tea tree essential oil from Melaleuca alternifolia as a sensory feed additive for all animal species, specifically as a flavouring compound. It sets out the conditions for its use, including maximum content levels in complete feed, and specifies requirements for handling and user protection due to potential health risks. The regulation also establishes transitional measures for products already on the market to adapt to the new requirements. The authorisation is valid until 6 August 2035.
The regulation consists of three articles and an annex. Article 1 authorises the use of tea tree essential oil as a feed additive under the conditions specified in the annex. Article 2 outlines transitional measures, allowing the continued use of existing stocks of the additive and related products produced and labelled before specific dates, ensuring a smooth transition to the new rules. Article 3 states that the regulation will enter into force twenty days after its publication in the Official Journal of the European Union. The annex specifies the identification number of the additive, its composition, the animal species for which it is authorised, and the maximum content levels. It also includes other provisions, such as the requirement for incorporation into feed as a premixture, storage and heat treatment instructions, and protective measures for users.
The most important provisions of this act are those related to the safety and handling of the additive. The regulation mandates that feed business operators establish operational procedures and organizational measures to address potential risks to users, including the use of personal protective equipment where risks cannot be eliminated. It also sets a maximum content limit for methyleugenol, a substance of concern found in tea tree essential oil, and allows for mixtures with other botanical additives only if the methyleugenol content remains below the specified limit. These measures are crucial for ensuring the safe use of the additive and protecting the health of both animals and users.
Commission Implementing Regulation (EU) 2025/1403 of 16 July 2025 concerning the authorisation of Spanish sage essential oil from Salvia officinalis ssp. lavandulifolia (Vahl) Gams and lavender essential oil from Lavandula angustifolia Mill. as feed additives for all animal species
This Commission Implementing Regulation (EU) 2025/1403 authorises the use of Spanish sage essential oil from Salvia officinalis ssp. lavandulifolia and lavender essential oil from Lavandula angustifolia as sensory feed additives (flavouring compounds) for all animal species. It establishes the conditions for their use, including maximum content levels in complete feed, and specifies labelling requirements to ensure safe handling and application. The regulation also provides transitional measures for products already on the market to adapt to the new requirements.
The regulation consists of three articles and an annex. Article 1 states that the substances specified in the Annex, belonging to the additive category ‘sensory additives’ and to the functional group ‘flavouring compounds’, are authorised as additives in animal nutrition, subject to the conditions laid down in that Annex. Article 2 defines transitional measures for feed additives Spanish sage essential oil from Salvia officinalis ssp. lavandulifolia (Vahl) Gams and lavender essential oil from Lavandula angustifolia Mill., as authorised pursuant to Directive 70/524/EEC and premixtures containing these additives. Article 3 states that this 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 of the feed additive, additive composition, analytical method, animal species, maximum content, and other provisions, including the end of the authorisation period. Compared to previous authorisations under Directive 70/524/EEC, this regulation provides more specific conditions of use, including maximum content levels and labelling requirements, based on the latest scientific advice from the European Food Safety Authority (EFSA).
Key provisions include the specific composition and characterisation of the authorised essential oils, maximum content levels for different animal species, and requirements for labelling of additives and premixtures. The regulation mandates that feed business operators establish operational procedures and organisational measures to address potential risks and, where necessary, provide personal protective equipment for users of the additives. It also specifies that the additives must be incorporated into feed in the form of a premixture and provides a transitional period for existing products to comply with the new labelling and usage conditions.
Decision No 1/2022 of the European Union-Canada Joint Customs Cooperation Committee concerning the mutual recognition of the Authorised Economic Operator Programme of the European Union and the Partners in Protection Programme of Canada [2025/1428]
This Decision of the EU-Canada Joint Customs Cooperation Committee (JCCC) establishes mutual recognition between the EU’s Authorised Economic Operator (AEO) programme and Canada’s Partners in Protection (PIP) programme. This means that the EU and Canada recognize each other’s supply chain security programs as equivalent, aiming to facilitate trade and enhance security. The decision outlines how the customs authorities will cooperate to maintain compatibility between their programs, exchange information, and provide reciprocal benefits to their respective program members. This agreement seeks to streamline processes for trusted traders, reduce inspections, and prioritize the handling of shipments from AEO and PIP members.
The Decision is structured into 9 articles covering definitions, mutual recognition, compatibility, benefits, information exchange, treatment of information, consultation and review, general acknowledgements, and final dispositions. It details the specific benefits that each Customs Authority will provide to the Programme Members of the other, such as favorable risk assessment, priority treatment for shipments, and business continuity mechanisms. It also establishes a framework for the exchange of information between customs authorities, including specific details about Programme Members, and sets out rules for the treatment of this information, including confidentiality and data protection measures. The Decision also provides for regular reviews and consultations to address any issues related to its implementation.
The most important provisions of this Decision relate to the benefits granted to Programme Members (Article 4) and the exchange and treatment of information (Articles 5 and 6). Article 4 ensures that AEO members in the EU and PIP members in Canada receive comparable benefits, such as reduced inspections and priority treatment, facilitating trade and reducing delays. Articles 5 and 6 establish a clear framework for the exchange of necessary information, including personal data, while ensuring its protection and confidentiality. These provisions are crucial for the effective implementation of the mutual recognition and for building trust between the EU and Canada in the area of customs cooperation.
