Commission Regulation (EC) No 1752/2002 of 1 October 2002 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 (Text with EEA relevance)
Date: 2002-10-01
Institutions: European Commission
Subjects: chemical product, health policy, manufactured feedingstuffs, material of animal origin, veterinary drug

L 264/18

EN

Official Journal of the European Communities

2.10.2002

COMMISSION REGULATION (EC) No 1752/2002

of 1 October 2002

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

(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 1181/2002 (2), and in parti-
cular Articles 6 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
concerned for the consumer of
foodstuffs of animal
origin and the impact of residues on the industrial
processing of foodstuffs.

the relevant

residues of

(5)

(6)

(7)

(8)

tional trade, and maximum residue limits should there-
fore also always be established for muscle or fat tissues.

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.

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

hydrochloride
Hydroxyethylsalicylate
should be inserted into Annex II to Regulation (EEC) No
2377/90.

and Xylazine

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 of the
European Parliament and of
to take
account of the provisions of this Regulation.

the Council (3)

(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:

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
liver or kidney. However,
the liver and kidney are
frequently removed from carcasses moving in interna-

Article 1

Annexes I and II 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 Communities.

It shall apply from the sixtieth day following its publication.

(1) OJ L 224, 18.8.1990, p. 1.
(2) OJ L 230, 28.8.2002, p. 3.

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

(1)

(2)

(3)

(4)

2.10.2002

EN

Official Journal of the European Communities

L 264/19

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

Done at Brussels, 1 October 2002.

For the Commission

Erkki LIIKANEN

Member of the Commission

A. The following substance is added to Annex I to Regulation (EEC) No 2377/90:

ANNEX

1.

Anti-infectious agents

1.2. Antibiotics

1.2.2. Cephalosporins

Pharmacologically active
substance(s)

‘Ceftiofur

Marker residue

Animal species

MRLs

Target tissues

Other provisions

Sum of all residues retain-
ing the betalactam struc-
ture expressed as desfur-
oylceftiofur

Bovine

1 000 µg/kg
2 000 µg/kg
2 000 µg/kg
6 000 µg/kg
100 µg/kg

Muscle
Fat
Liver
Kidney
Milk’

B. The following substances are added to Annex II to Regulation (EEC) No 2377/90:

2.

Organic compounds

Pharmacologically active substance(s)

Animal species

Other provisions

‘Hydroxyethylsalicylate

Xylazine hydrochloride

All food producing species except fish

For topical use only’

Bovine, equidae

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