Skip to main content
PolicySpeak
← All legislative files

Pharmacologically Active Substances Residue Limits Regulation

Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, and repealing Regulation (EEC) No 2377/90

Stage
In force
In force
In force since 6 Jul 2009 · CELEX 32009R0470
Procedure
Regulation
Last activity
6 May 2009
18 acts

Delegated and implementing acts beneath it

By status: 18 published.

ActKindStatusAdoption
Commission Implementing Regulation (EU) 2025/1908Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2025/1105Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2025/1101ImplementingPublished
Commission Implementing Regulation (EU) 2025/1102Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2025/1103Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2024/2858ImplementingPublished
Commission Implementing Regulation (EU) 2024/859Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2024/860Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2023/2203Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2023/2194Implementing · RegulationPublishedQ4 2023
Commission Implementing Regulation (EU) 2023/981Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2023/454Implementing · RegulationPublished
Commission Implementing Regulation (EU) 2023/411ImplementingPublished
Commission Implementing Regulation (EU) 2022/634Implementing · RegulationPublished
Commission Delegated Regulation (EU) 2019/157Implementing · RegulationPublished
Commission Delegated Regulation (EU) 2016/1969Implementing · RegulationPublishedQ4 2018
Commission Delegated Regulation (EU) 2013/1002Implementing · RegulationPublished
Commission Delegated Directive (EU) 2014/3Implementing · RegulationPublished

Titles link to EUR-Lex where the act has been published.

Summary

Generated

This regulation establishes EU-wide procedures for setting maximum residue limits (MRLs) for pharmacologically active substances in food of animal origin, replacing the 1990 framework. It affects veterinary pharmaceutical companies, food producers, and national food safety authorities monitoring residues in meat, milk, eggs, and honey.

What the workspace adds on this file

Everything above is the public record. Subscribers see this page with their own layer on top.

Why it matters to you

What this file means for your organization, assessed against your own priorities.

What moved

When this file moves, it reaches your own briefing, with a link to its source.

Your contacts on it

Your team's contacts logged against this file: who you met, what was said and the next step.

A first draft

A statement, a member update or a meeting brief on this file, in your organization's voice, with its sources.

Sources: EUR-Lex. Record as of 14 Sept 2026. Something wrong on this page? Report an error.

Request access

See this file with your own layer on top: why it matters to you, your contacts on it and a first draft. We’ll schedule a 20-minute walkthrough.

EU-hosted · GDPR-compliant · Trust Center →

By submitting, you agree to our privacy policy.