Veterinary Medicines Regulations 2013 (S.I. No. 2033 of 2013).
Type of law
The Regulations make provision for the authorisation, manufacture, classification, distribution and administration of veterinary medicinal products. The Regulations, among other things: regulate the supply and possession of veterinary medicinal products, and introduce new classifications of those products; require a marketing authorization of the Secretary of State for the placing on the market of a veterinary medicinal product; require manufacturers to obtain a manufacturing authorization; provide for control on importation of a veterinary medicinal product; provide for control of medicated feedingstuffs and feedingstuffs containing specified additives; continue the Veterinary Products Committee; provide for appeals to the Veterinary Products Committee; create administrative arrangements for the enforcement of the Regulations; and define offences.
Date of text
Regulation (EC) No. 470/2009 of the European Parliament and of the Council 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.
Regulation (EC) No. 767/2009 of the European Parliament and of the Council on the placing on the market and use of feed, amending European Parliament and Council Regulation (EC) No. 1831/2003 and repealing Council Directive 79/373/EEC, Commission Directive 80/511/EEC, Council Directives 82/471/EEC, 83/228/EEC, 93/74/EEC, 93/113/EC and 96/25/EC and Commission Decision 2004/217/EC.