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Commission Implementing Regulation (EU) 2015/262

Preamble
Recitals 78
Chapter I - SUBJECT MATTER, SCOPE, DEFINITIONS, GENERAL PRINCIPLES (Article 1-4) 4
Chapter II - IDENTIFICATION OF EQUIDAE BORN IN THE UNION (Article 5-13) 9
Chapter III - IDENTIFICATION OF EQUIDAE IMPORTED INTO THE UNION (Article 14-15) 2
Chapter IV - CHECKS REQUIRED PRIOR TO ISSUING OF IDENTIFICATION DOCUMENTS AND METHODS OF IDENTITY VERIFICATION (Article 16-22) 7
Chapter V - MOVEMENT AND TRANSPORT OF EQUIDAE (Article 23-26) 4
Chapter VI - MANAGEMENT, DUPLICATION, REPLACEMENT AND SUSPENSION OF IDENTIFICATION DOCUMENTS (Article 27-33) 7
Chapter VII - DEATH OF EQUIDAE AND EQUIDAE INTENDED FOR SLAUGHTER FOR HUMAN CONSUMPTION AND MEDICATION RECORD (Article 34-37) 4
Chapter VIII - RECORDS AND PENALTIES (Article 38-41) 4
Chapter IX - TRANSITIONAL AND FINAL PROVISIONS (Article 42-44) 3
Annexes 3

Recital 56

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Recital 56

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(56)Point (b) of Article 2 of Regulation (EC) No 470/2009 of the European Parliament and of the Council ³² defines food producing animals as ‘animals bred, raised, kept, slaughtered or harvested for the purposes of producing food’. Article 16 of that Regulation provides that only pharmacologically active substances which are classified in accordance with Article 14(2)(a), (b) or (c) of that Regulation may be administered to food-producing animals within the Union provided that such administration is in accordance with Directive 2001/82/EC of the European Parliament and of the Council ³³ .

32 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 ( OJ L 152, 16.6.2009, p. 11 ). ↩
33 Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products ( OJ L 311, 28.11.2001, p. 1 ). ↩

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