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WTO notification · SPS

European UnionUpdated: check whether it is now adopted or in force

Animal products, food – European Union

Official title

Commission Implementing Regulation (EU) amending Regulation (EU) No 37/2010 as regards the classification of the substance fluralaner with respect to its maximum residue limit in foodstuffs of animal origin

The European Union issued an addendum on 2 October 2025 to the earlier SPS notification G/SPS/N/EU/847. Addenda often report that a measure was adopted, changed, postponed or withdrawn. The measure was first notified on 29 April 2025. The comment period closed on 28 June 2025.

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Source: WTO ePing (opens in a new tab). Summaries by Expodite, which is independent of the WTO.

Published here:

Updated here:

At a glance

Products

Foodstuffs of animal origin

Notifying member
European Union
Status
Updated: check whether it is now adopted or in force
Objectives
  • Food safety
  • Animal health
Area
SPS: Food safety, animal and plant healthSanitary and phytosanitary measures
Notification type
Regular notification
Document symbol
G/SPS/N/EU/847Latest notice: G/SPS/N/EU/847/Add.1
Keywords
Human health, Animal health, Food safety, Animal diseases, Maximum residue limits (MRLs), Adoption/publication/entry into force of reg.

Key dates

Distributed by the WTO
Comment deadline
Closed on 28 June 2025
Proposed adoption
July 2025
Proposed entry into force
This Regulation shall enter into force on the twentieth day following its publication in the Official Journal of the European Union.

How to comment

The comment period closed on 28 June 2025. You can still raise concerns about the measure with your country's WTO SPS enquiry point, quoting the document symbol G/SPS/N/EU/847/Add.1; it can take them up with the European Union.

Find your country's enquiry point on WTO ePing (opens in a new tab)

What the notification says

Latest notice (⁨G/SPS/N/EU/847/Add.1⁩, 2 October 2025)

Classification of the substance fluralaner with respect to its maximum residue limit in foodstuffs of animal origin

The proposal notified in G/SPS/N/EU/847 (29 April 2025) is now adopted by Commission Implementing Regulation (EU) 2025/1908 of 24 September 2025 amending Regulation (EU) No 37/2010 as regards the classification of the substance fluralaner with respect to its maximum residue limit in foodstuffs of animal origin (Text with EEA relevance). This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.

This draft legislation will establish a maximum residue limit (MRL) in the Union for the pharmacologically active substance fluralaner, intended for use in veterinary medicinal products for food-producing animals. This draft legislation will amend the existing entry for fluralaner in Table 1 of the Annex of Commission Regulation (EU) No 37/2010 on pharmacologically active substances and its classification regarding maximum residue limits in foodstuffs of animal origin.

Notices on this measure

Every notice about this measure published here, newest first. Each one is the notifying member's own text.

  1. AddendumG/SPS/N/EU/847/Add.1

    Classification of the substance fluralaner with respect to its maximum residue limit in foodstuffs of animal origin

    The proposal notified in G/SPS/N/EU/847 (29 April 2025) is now adopted by Commission Implementing Regulation (EU) 2025/1908 of 24 September 2025 amending Regulation (EU) No 37/2010 as regards the classification of the substance fluralaner with respect to its maximum residue limit in foodstuffs of animal origin (Text with EEA relevance). This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.

  2. Regular notificationG/SPS/N/EU/847

    Comment deadline: Closed on 28 June 2025

    Commission Implementing Regulation (EU) amending Regulation (EU) No 37/2010 as regards the classification of the substance fluralaner with respect to its maximum residue limit in foodstuffs of animal origin

    This draft legislation will establish a maximum residue limit (MRL) in the Union for the pharmacologically active substance fluralaner, intended for use in veterinary medicinal products for food-producing animals. This draft legislation will amend the existing entry for fluralaner in Table 1 of the Annex of Commission Regulation (EU) No 37/2010 on pharmacologically active substances and its classification regarding maximum residue limits in foodstuffs of animal origin.

All updates from the European Union
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    Symbol: G/TBT/N/EU/1250Comments until 1 January 2027

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