Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 Ma... (32009R0470)
INHALT
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 )
- 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)
- 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
Feedback