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Commission Regulation (EC) No. 205/2006 amending Annexes I and II to Council Regulation (EEC) No. 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards toltrazuril, diethylene glycol monoethyl ether and polyoxyethylene sorbitan monooleate.

Country/Territory
European Union
Document type
Regulation
Date
2006
Source
FAO, FAOLEX
Original source
Official Journal of the European Union L 34, 7 February 2006, pp. 21-23.
Subject
Food & nutrition
Keyword
Food quality control/food safety MRL-maximum residue limit Drugs
Geographical area
European Union Countries
Abstract

All pharmacologically active substances used within the Community in veterinary medicinal products intended for administration to animals for the purpose of producing foodstuffs must be evaluated in accordance with Regulation (EEC) No. 2377/90. Annexes I and II to that Regulation are supplemented by inserting certain veterinary medicinal products (namely toltrazuril, diethylene glycol monoethyl ether and polyoxyethylene sorbitan monooleate) and their respective maximum residue limits in the list of pharmacologically active substances.

Full text
English
Website
europa.eu

References - Legislation

Amends

Council Regulation (EEC) No. 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin.

Legislation | European Union | 1990

Keyword: Food quality control/food safety, MRL-maximum residue limit, Drugs

Source: FAO, FAOLEX