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Veterinary Medicines Regulations 2011 (S.I. No. 2159 of 2011).

This content is exclusively provided by FAO / FAOLEX / ECOLEX

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.
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 importa
Title:
Veterinary Medicines Regulations 2011 (S.I. No. 2159 of 2011).
Country:
United Kingdom of Great Britain and Northern Ireland
Type of document:
Regulation
Date of text:
2011
Data source:
FAO, FAOLEX
ECOLEX regions:
Europe
European Union Countries
Northern Europe
ECOLEX URL:
ECOLEX
Files:
uk109951.pdf
Repealed:
Yes
Amended by
Implements
Council Directive 90/167/EEC laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the Community.
Commission Directive 91/412/EEC laying down the principles and guidelines of good manufacturing practice for veterinary medicinal products.
Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products.
Regulation (EC) No. 178/2002 of the European Parliament and of the Council laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety
Regulation (EC) No. 1831/2003 of the European Parliament and of the Council on additives for use in animal nutrition.
Regulation (EC) No. 882/2004 of the European Parliament and of the Council on official controls performed to ensure the verification of compliance with feed and food law, animal health and animal welfare rules.
Regulation (EC) No. 183/2005 of the European Parliament and of the Council laying down requirements for feed hygiene.
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.
Commission Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin.
Repeals
Veterinary Medicines Regulations 2009 (S.I. No. 2297 of 2009).
Repealed by