Regulation (EU) 2019/4 of the European Parliament and of the Council of 11 Decemb... (32019R0004)
Regulation (EU) 2019/4 of the European Parliament and of the Council of 11 December 2018 on the manufacture, placing on the market and use of medicated feed, amending Regulation (EC) No 183/2005 of the European Parliament and of the Council and repealing Council Directive 90/167/EEC (Text with EEA relevance)
- REGULATION (EU) 2019/4 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
- of 11 December 2018
- on the manufacture, placing on the market and use of medicated feed, amending Regulation (EC) No 183/2005 of the European Parliament and of the Council and repealing Council Directive 90/167/EEC
- (Text with EEA relevance)
- CHAPTER I
- SUBJECT MATTER, SCOPE AND DEFINITIONS
- Article 1
- Subject matter
- Article 2
- Scope
- Article 3
- Definitions
- CHAPTER II
- MANUFACTURE, STORAGE, TRANSPORT AND PLACING ON THE MARKET
- Article 4
- General obligations
- Article 5
- Composition
- Article 6
- Homogeneity
- Article 7
- Cross-contamination
- Article 8
- Anticipated production
- Article 9
- Specific labelling requirements
- Article 10
- Packaging
- Article 11
- Advertising of medicated feed and intermediate products
- Article 12
- Intra-Union trade and import
- CHAPTER III
- APPROVAL OF ESTABLISHMENTS
- Article 13
- Approval obligations
- Article 14
- Lists of approved establishments
- Article 15
- Transitional measures concerning the implementation of the requirements for approval and registration
- CHAPTER IV
- PRESCRIPTION AND USE
- Article 16
- Prescription
- Article 17
- Use of medicated feed
- Article 18
- Collection or discard systems of unused or expired products
- CHAPTER V
- PROCEDURAL AND FINAL PROVISIONS
- Article 19
- Amendment of Annexes
- Article 20
- Exercise of the delegation
- Article 21
- Committee procedure
- Article 22
- Penalties
- Article 23
- Amendment to Regulation (EC) No 183/2005
- Article 24
- Transitional measures
- Article 25
- Repeal
- Article 26
- Entry into force and application
- ANNEX I
- SPECIFIC REQUIREMENTS FOR FEED BUSINESS OPERATORS IN ACCORDANCE WITH ARTICLE 4
- SECTION 1
- Facilities and equipment
- SECTION 2
- Personnel
- SECTION 3
- Manufacture
- SECTION 4
- Quality control
- SECTION 5
- Storage and transport
- SECTION 6
- Record-keeping
- SECTION 7
- Complaints and product recall
- SECTION 8
- Additional requirements for mobile mixers
- ANNEX II
- ANNEX III
- SPECIFIC LABELLING REQUIREMENTS REFERRED TO IN ARTICLE 9(1)
- ANNEX IV
- PERMITTED TOLERANCES FOR THE COMPOSITIONAL LABELLING OF MEDICATED FEED OR INTERMEDIATE PRODUCTS AS REFERRED TO IN ARTICLE 9(3)
- ANNEX V
- INFORMATION TO BE INCLUDED IN THE VETERINARY PRESCRIPTION FOR MEDICATED FEED AS REFERRED TO IN ARTICLE 16(6)
- VETERINARY PRESCRIPTION FOR MEDICATED FEED
- ANNEX VI
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