Veterinary Medicines Regulations 2011 (S.I. No. 2159 of 2011).
Type of law
The Regulations make provision for the authorization, 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 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; and continue the Veterinary Products Committee.
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.