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Veterinary Medicines Regulations 2013 (S.I. No. 2033 of 2013).

Country
United Kingdom of Great Britain and Northern Ireland
Type of law
Regulation
Source
FAO , FAOLEX
Abstract
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.
Attached files
http://faolex.fao.org/docs/pdf/uk127461.pdf
Web site
http://www.opsi.gov.uk
Date of text
Repealed
No
Source language

English

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