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Commission Implementing Decision (EU) 2025/357 of 21 February 2025 not approving 5-chloro-2-methyl-2H-isothiazol-3-one (CIT) as an active substance for use in biocidal products of product-type 6 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

Bill Healthcare & Pharma PUBLISHED
Date: 24th Feb, 2025 Source: Register of Delegated and Implementing Acts Country: European Union Original Source

Brief

The Commission Implementing Regulation (EU) 2024/2563 amends Implementing Regulation (EU) 2022/1646 to clarify content and submission requirements for national risk-based control plans and surveillance plans. This regulation aims to provide a consistent approach to monitoring and reporting non-compliance data, ensuring that Member States submit accurate information on follow-up measures taken by competent authorities. The main purpose of this regulation is to ensure the consistency and accuracy of the national risk-based control plans and surveillance plans submitted by Member States.

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Register of Delegated and Implementing Acts

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