EUR-Lex Access to European Union law

Back to EUR-Lex homepage

This document is an excerpt from the EUR-Lex website

Document 32003R2011

Commission Regulation (EC) No 2011/2003 of 14 November 2003 amending Annexes I and III 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 (Text with EEA relevance)

OJ L 297, 15.11.2003, p. 15–18 (ES, DA, DE, EL, EN, FR, IT, NL, PT, FI, SV)
Special edition in Czech: Chapter 03 Volume 040 P. 509 - 512
Special edition in Estonian: Chapter 03 Volume 040 P. 509 - 512
Special edition in Latvian: Chapter 03 Volume 040 P. 509 - 512
Special edition in Lithuanian: Chapter 03 Volume 040 P. 509 - 512
Special edition in Hungarian Chapter 03 Volume 040 P. 509 - 512
Special edition in Maltese: Chapter 03 Volume 040 P. 509 - 512
Special edition in Polish: Chapter 03 Volume 040 P. 509 - 512
Special edition in Slovak: Chapter 03 Volume 040 P. 509 - 512
Special edition in Slovene: Chapter 03 Volume 040 P. 509 - 512
Special edition in Bulgarian: Chapter 03 Volume 050 P. 131 - 134
Special edition in Romanian: Chapter 03 Volume 050 P. 131 - 134

No longer in force, Date of end of validity: 05/07/2009; Implicitly repealed by 32009R0470

ELI: http://data.europa.eu/eli/reg/2003/2011/oj

32003R2011

Commission Regulation (EC) No 2011/2003 of 14 November 2003 amending Annexes I and III 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 (Text with EEA relevance)

Official Journal L 297 , 15/11/2003 P. 0015 - 0018


Commission Regulation (EC) No 2011/2003

of 14 November 2003

amending Annexes I and III 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

(Text with EEA relevance)

THE COMMISSION OF THE EUROPEAN COMMUNITIES,

Having regard to the Treaty establishing the European Community,

Having regard to Council Regulation (EEC) No 2377/90 of 26 June 1990 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin(1), as last amended by Commission Regulation (EC) No 1873/2003(2), and in particular Articles 6, 7 and 8 thereof,

Whereas:

(1) In accordance with Regulation (EEC) No 2377/90, maximum residue limits must be established progressively for all pharmacologically active substances which are used within the Community in veterinary medicinal products intended for administration to food-producing animals.

(2) Maximum residue limits should be established only after the examination within the Committee for Veterinary Medicinal Products of all the relevant information concerning the safety of residues of the substance concerned for the consumer of foodstuffs of animal origin and the impact of residues on the industrial processing of foodstuffs.

(3) In establishing maximum residue limits for residues of veterinary medicinal products in foodstuffs of animal origin, it is necessary to specify the animal species in which residues may be present, the levels which may be present in each of the relevant meat tissues obtained from the treated animal (target tissue) and the nature of the residue which is relevant for the monitoring of residues (marker residue).

(4) For the control of residues, as provided for in appropriate Community legislation, maximum residue limits should usually be established for the target tissues of liver or kidney. However, the liver and kidney are frequently removed from carcases moving in international trade, and maximum residue limits should therefore also always be established for muscle or fat tissues.

(5) In the case of veterinary medicinal products intended for use in laying birds, lactating animals or honey bees, maximum residue limits must also be established for eggs, milk or honey.

(6) Alphacypermethrin and Metamizole should be inserted into Annex I to Regulation (EEC) No 2377/90.

(7) In order to allow for the completion of scientific studies, Phoxim should be inserted into Annex III to Regulation (EEC) No 2377/90.

(8) An adequate period should be allowed before the entry into force of this Regulation in order to allow Member States to make any adjustment which may be necessary to the authorisations to place the veterinary medicinal products concerned on the market which have been granted in accordance with Directive 2001/82/EC(3) of the European Parliament and of the Council to take account of the provisions of this Regulation.

(9) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Veterinary Medicinal Products,

HAS ADOPTED THE FOLLOWING REGULATION:

Article 1

Annexes I and III to Regulation (EEC) No 2377/90 are hereby amended as set out in the Annex hereto.

Article 2

This Regulation shall enter into force on the third day following its publication in the Official Journal of the European Union.

It shall apply from the 60th day following its publication.

This Regulation shall be binding in its entirety and directly applicable in all Member States.

Done at Brussels, 14 November 2003.

For the Commission

Erkki Liikanen

Member of the Commission

(1) OJ L 224, 18.8.1990, p. 1.

(2) OJ L 275, 25.10.2003, p. 9.

(3) OJ L 311, 28.11.2001, p. 1.

ANNEX

A. Annex I to Regulation (EEC) No 2377/90 is amended as follows:

2. Antiparasitic agents

2.2. Agents acting against ectoparasites

2.2.3. Pyrethroids

">TABLE>"

4. Anti-inflammatory agents

4.1. Nonsteroidal anti-inflammatory agents

4.1.5. Pyrazolone derivatives

">TABLE>"

B. Annex III to Regulation (EEC) No 2377/90 is amended as follows:

2. Antiparasitic agents

2.2. Agents acting against ectoparasites

2.2.4. Organophosphates

">TABLE>"

Top