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Regulation (EU) 2022/839 of the European Parliament and of the Council of 30 May 2022 laying down transitional rules for the packaging and labelling of veterinary medicinal products authorised or registered in accordance with Directive 2001/82/EC or Regulation (EC) No 726/2004 (Text with EEA relevance) article 1 CELEX: 32022R0839 Definitions
For the purposes of this Regulation, the following definitions apply: (1) ‘veterinary medicinal product’ means a veterinary medicinal product as defined in Article 4, point (1), of Regulation (EU) 2019/6; (2) ‘labelling’ means labelling as defined in Article 4, point (24), of Regulation (EU) 2019/6; (3) ‘package leaflet’ means a package leaflet as defined in Article 4, point (27), of Regulation (EU) 2019/6; (4) ‘placing on the market’ means placing on the market as defined in Article 4, point (35), of Regulation (EU) 2019/6. |