European Parliament 6 May 2009, Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance )

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European Union · · · Cited by 1,031 · 16-06-2009

TITLE I. GENERAL PROVISIONS
Article 1. Subject matter and scope
Article 2. Definitions
TITLE II. MAXIMUM RESIDUE LIMITS
CHAPTER I. Risk assessment and risk management
Section 1. Pharmacologically active substances intended for use in veterinary medicinal products in the Community
Article 3. Application for an opinion of the Agency
Article 4. Opinion of the Agency
Article 5. Extrapolation
Article 6. Scientific risk assessment
Article 7. Risk management recommendations
Article 8. Applications and procedures
Section 2. Other pharmacologically active substances for which an opinion of the Agency may be requested
Article 9. Opinion of the Agency requested by the Commission or a Member State
Article 10. Pharmacologically active substances contained in biocidal products used in animal husbandry
Section 3. Common provisions
Article 11. Review of an opinion
Article 12. Publication of opinions
Article 13. Implementing measures
CHAPTER II. Classification
Article 14. Classification of pharmacologically active substances
Article 15. Accelerated procedure for an opinion of the Agency
Article 16. Administration of substances to food-producing animals
Article 17. Procedure
TITLE III. REFERENCE POINTS FOR ACTION
Article 18. Establishment and review
Article 19. Methods for establishing reference points for action
Article 20. Community contribution to the support measures for reference points for action
TITLE IV. MISCELLANEOUS PROVISIONS
Article 21. Analytical methods
Article 22. Circulation of foodstuffs
Article 23. Placing on the market
Article 24. Action in case of confirmed presence of a prohibited or non-authorised substance
TITLE V. FINAL PROVISIONS
Article 25. Standing Committee on Veterinary Medicinal Products
Article 26. Standing Committee on the Food Chain and Animal Health
Article 27. Classification of pharmacologically active substances under Regulation (EEC) No 2377/90
Article 28. Reporting
Article 29. Repeal
Article 30. Amendments to Directive 2001/82/EC
Article 31. Amendment to Regulation (EC) No 726/2004
Article 32. Entry into force

16.6.2009

Official Journal of the European Union

L 152/11

REGULATION (EC) No 470/2009 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL

of 6 May 2009

laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of

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