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By way of derogation from point (h) of Article 3(2) and paragraph 2 of this Article, a Member State may allow a veterinary prescription for medicated feed to be issued by a professional person qualified to do so in accordance with applicable national law on 27 January 2019.
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(3) Council Directive 90/167/EEC of 26 March 1990 laying...
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(3) The pursuit of a high level of protection of human...
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Animal by-products derived from category 2 and 3 material – except for blood, hides and skins, hooves, feathers, wool, horns, hair and fur from animals unfit for human consumption but not showing any signs of a communicable disease – may be used for the feeding of the following animals:
20 maj 2024 · special rules on medicated feed containing immunological veterinary medicinal products and antiparasitics. Contributes to the EU’s action to fight antimicrobial resistance: bans the use of antimicrobials via medicated feed for prophylaxis and growth promotion;
SECTION 3 Manufacture . 1. Feed business operators shall take account of requirements under relevant... 2. Medicated feed and intermediate products shall be stored separately from... 3....
4 4. AUTHORISATION OF GENERIC FEED ADDITIVES For feed additives that are not linked to a specific authorisation holder (i.e. feed additives other than those referred to in section 3) ("generic feed additives")13 the following applies: According to Article 4(3) of Regulation (EC) No 1831/2003, an applicant for
Medicated feed is a specific form of compound feed, which is often produced in the same plant as conventional compound feed. Therefore, the manufacturing, storage and delivery have to comply with EU legal feed hygiene requirements as laid down in Regulation (EC) No 183/2005.
25 maj 2023 · • Annex X, chapter 2, section 10 of Reg (EU) No 142/2011 (Specific requirements for feeding to farmed animals, other than fur animals, of certain Category 3 material referred to Article 10(f) of Regulation
