Commission Implementing Regulation (EU) 2022/1646 of 23 September 2022 on uniform... (32022R1646)
INHALT
Commission Implementing Regulation (EU) 2022/1646 of 23 September 2022 on uniform practical arrangements for the performance of official controls as regards the use of pharmacologically active substances authorised as veterinary medicinal products or as feed additives and of prohibited or unauthorised pharmacologically active substances and residues thereof, on specific content of multi-annual national control plans and specific arrangements for their preparation (Text with EEA relevance)
- COMMISSION IMPLEMENTING REGULATION (EU) 2022/1646
- of 23 September 2022
- on uniform practical arrangements for the performance of official controls as regards the use of pharmacologically active substances authorised as veterinary medicinal products or as feed additives and of prohibited or unauthorised pharmacologically active substances and residues thereof, on specific content of multi-annual national control plans and specific arrangements for their preparation
- (Text with EEA relevance)
- CHAPTER I
- SUBJECT MATTER, SCOPE AND DEFINITIONS
- Article 1
- Subject matter
- Article 2
- Definitions
- CHAPTER II
- SPECIFIC ADDITIONAL CONTENT OF THE MANCP
- Article 3
- General provisions
- Article 4
- National risk-based control plan for production in the Member States
- Article 5
- National randomised surveillance plan for production in the Member States
- Article 6
- National risk-based control plan for third-country imports
- Article 7
- Additional content of the national risk-based control plans and randomised surveillance plan
- CHAPTER III
- SUBMISSION AND EVALUATION OF THE PLANS AND SUBMISSION OF DATA BY THE MEMBER STATES
- Article 8
- Submission and evaluation of the control plans
- Article 9
- Submission of data by the Member State
- CHAPTER IV
- GENERAL PROVISIONS
- Article 10
- Repeal of Decision 97/747/EC
- Article 11
- References
- Article 12
- Entry into force and application
- ANNEX I
- Minimum sampling frequency per Member State in the national risk-based control plan for production in the Member States (as referred to in Article 4(c))
- Additional provisions
- ANNEX II
- Minimum sampling frequency per Member State in the national randomised surveillance plan for production in the Member States (as referred to in Article 5(c))
- Additional provisions:
- ANNEX III
- Minimum sampling frequency per Member State in the national risk-based control plan for third-country imports (as referred to in Article 6(c))
- Additional provisions:
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