Here’s a breakdown of the EU legal acts you provided, focusing on their core content:
Commission Delegated Regulation (EU) 2026/109
This regulation amends and corrects Delegated Regulation (EU) 2019/1122. It concerns the functioning of the Union Registry under Regulation (EU) 2018/842, which deals with greenhouse gas emission reductions. The amendment takes into account subsequent changes introduced by Regulation (EU) 2023/857. In essence, it fine-tunes the operational details of the registry used to track emission reduction efforts across the EU.
Commission Delegated Regulation (EU) 2026/81
This regulation amends Delegated Regulation (EU) 2019/1122, focusing on the Union Registry’s operation in accordance with Regulation (EU) 2018/841. Regulation 2018/841 addresses greenhouse gas emissions from land use, land use change and forestry. Therefore, this act adjusts the registry’s function to properly account for emissions and removals in the land sector.
Commission Implementing Regulation (EU) 2026/765
This regulation establishes the methods for sampling and analysis, and the interpretation of results, for official controls of pesticide residues in food and feed. It applies to both plant and animal products. Crucially, it repeals Directive 2002/63/EC, providing updated and harmonized procedures for monitoring pesticide levels across the EU food chain.
Commission Implementing Regulation (EU) 2026/814
This regulation amends Annexes V and XIV to Implementing Regulation (EU) 2021/404. It concerns the listing of third countries (Chile, the United Kingdom, and the United States) authorized for the entry into the EU of consignments of poultry and poultry products, including fresh meat. This means the regulation adjusts the list of countries from which the EU permits imports of these products, based on factors like animal health and safety standards.
Commission Implementing Regulation (EU) 2026/758
This regulation amends Implementing Regulation (EU) 2021/17. The core focus is on simplifying the process for variations to marketing authorizations for medicinal products. Specifically, it adds the inclusion of a variation amending the contact details of the distributor to the list of variations not requiring assessment. This streamlines administrative procedures for minor changes related to distribution information.
