Commission Regulation (EC) No 324/2004 of 25 February 2004 amending Annex I 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)
Date: 2004-02-25
Institutions: European Commission
Subjects: animal product, foodstuffs legislation, veterinary drug

L 58/16

EN

Official Journal of the European Union

26.2.2004

COMMISSION REGULATION (EC) No 324/2004

of 25 February 2004

amending Annex I 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 estab-
lishment of maximum residue limits of veterinary medicinal
products in foodstuffs of animal origin (1), as last amended by
Commission Regulation (EC) No 2145/2003 (2), and in particu-
lar Articles 6, 7 and 8 thereof,

Whereas:

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

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

the relevant

residues of

(5)

(6)

(7)

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.

Kanamycin and diclofenac should be inserted into
Annex I to Regulation (EEC) No 2377/90.

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.

(8)

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

HAS ADOPTED THIS REGULATION:

Article 1

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 resi-
dues (marker residue).

For the control of residues, as provided for in appro-
priate Community legislation, maximum residue limits
should usually be established for the target tissues of
the liver and kidney are
liver or kidney. However,
frequently removed from carcasses moving in interna-
tional trade, and maximum residue limits should there-
fore also always be established for muscle or fat tissues.

Annex I to Regulation (EEC) No 2377/90 is 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.

(1) OJ L 224, 18.8.1990, p. 1.
(2) OJ L 322, 9.12.2003, p. 5.

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

(1)

(2)

(3)

(4)

26.2.2004

EN

Official Journal of the European Union

L 58/17

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

Done at Brussels, 25 February 2004.

For the Commission

Erkki LIIKANEN

Member of the Commission

The following substances are inserted in Annex I to Regulation (EEC) No 2377/90

ANNEX

1.

Anti-infectious agents

1.2.

Antibiotics

1.2.10. Aminoglycosides

Pharmacologically active substance(s)

Marker residue

Animal species

‘Kanamycin

Kanamycin A

All food producing species except fish (1)

(1) Not for use in animals from which eggs are produced for human consumption.
(2) For porcine and poultry species this MRL relates to “skin and fat in natural proportions”.’

4.

Anti-inflammatory agents

4.1.

Non-steroidal anti-inflammatory agents

4.1.6.

Phenyl acetic acid derivatives

Pharmacologically active substance(s)

Marker residue

Animal species

‘diclofenac

diclofenac

Bovine (1)

Porcine

(1) Not for use in animals from which milk is produced for human consumption.’

Target tissues

MRLs

100 µg/kg
100 µg/kg
600 µg/kg
2 500 µg/kg
150 µg/kg

Muscle

Fat (2)

Liver

Kidney

Milk

Target tissues

MRLs

5 µg/kg
1 µg/kg
5 µg/kg
10 µg/kg
5 µg/kg
1 µg/kg
5 µg/kg
10 µg/kg

Muscle

Fat

Liver

Kidney

Muscle

Skin + fat

Liver

Kidney

L

5
8
/
1
8

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2
6
2
2
0
0
4