Commission Implementing Regulation (EU) 2022/1646 CHAPTER I — SUBJECT MATTER, SCOPE AND DEFINITIONS

Article 1–Article 2 · 2 articles

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Subject matter

Article 1

For the purpose of official controls on 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, this Regulation lays down the following: (a) the annual uniform minimum sampling frequency as part of official controls, having regard to the hazards and risks related to the substances concerned; (b) specific additional arrangements and specific additional content for the Member States’ multi-annual national control plan (‘MANCP’), in addition to those provided for in Article 110 of Regulation (EU) 2017/625.

Definitions

Article 2

For the purposes of this Regulation, the definitions in Regulation (EC) No 178/2002, Commission Delegated Regulation (EU) 2019/2090 ( 9 ) , Implementing Regulation (EU) 2021/808 and Delegated Regulation (EU) 2022/1644 apply.

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