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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 )- Recitals
TITLE I — GENERAL PROVISIONS- TITLE II — MAXIMUM RESIDUE LIMITS
- CHAPTER I — Risk assessment and risk management
- CHAPTER II — Classification
- TITLE III — REFERENCE POINTS FOR ACTION
- TITLE IV — MISCELLANEOUS PROVISIONS
- 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
- Final