European Commission 23 September 2022, 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)

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European Union · · · Cited by 30 · 23-09-2022

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))

26.9.2022

Official Journal of the European Union

L 248/32

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

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