Commission Regulation (EC) No 270/97 of 14 February 1997 amending Annex I, II, III and IV of 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
Date: 1997-02-14
Institutions: European Commission
Subjects: animal product, food inspection, health control, veterinary drug, waste








L_1997045EN.01000801.xml










15.2.1997   


EN


Official Journal of the European Communities


L 45/8





COMMISSION REGULATION (EC) No 270/97
of 14 February 1997
amending Annex I, II, III and IV of 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
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 211/97 (2), and in particular Articles 6, 7 and 8 thereof,
Whereas, 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;
Whereas 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;
Whereas, 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);
Whereas, 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, whereas, however, the liver and kidney are frequently removed from carcasses moving in international trade, and maximum residue limits should therefore also always be established for muscle or fat tissues;
Whereas, 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;
Whereas, doramectin and cefazolin (for milk) should be inserted into Annex I to Regulation (EEC) No 2377/90;
Whereas alfaprostol, cefazolin, medroxyprogesterone acetate and propylene glycol should be inserted into Annex II to Regulation (EEC) No 2377/90;
Whereas, in order to allow for the completion of scientific studies, cephapirin should be inserted into Annex III to Regulation (EEC) No 2377/90;
Whereas it appears that maximum residue limits cannot be established for chloroform because residues, at whatever limit, in foodstuffs of animal origin constitute a hazard to the health of the consumer; whereas chloroform should therefore be inserted into Annex IV to Regulation (EEC) No 2377/90;
Whereas a period of 60 days 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 Council Directive 81/851/EEC (3), as last amended by Directive 93/40/EEC (4), to take account of the provisions of this Regulation;
Whereas 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
Annex I, II, III and IV of 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 sixtieth day following its publication in the Official Journal of the European Communities.

This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 14 February 1997.


For the Commission

Martin BANGEMANN

Member of the Commission





(1)  OJ No L 224, 18. 8. 1990, p. 1.

(2)  OJ No L 35, 5. 2. 1997, p. 1.

(3)  OJ No L 317, 6. 11. 1981, p. 1.

(4)  OJ No L 214, 24. 8. 1993, p. 31.


ANNEX






A.


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






1.


Anti-infectious agents






1.2.


Antibiotics






1.2.2.


Cephalosporins










Pharmacologically active substance


Marker residue


Animal species


MRLs


Target tissues


Other provisions










‘1.2.2.2.


Cefazolin






Cefazolin


Bovine


50 μg/kg


Milk’


 






















2.


Anti-parasitic agents






2.3.


Agents acting against endo- and ectoparasites






2.3.1.


Avermectins










Pharmacologically active substance


Marker residue


Animal species


MRLs


Target tissues


Other provisions










‘2.3.1.3.


Doramectin






Doramectin


Bovine


150 μg/kg


Fat


 




100 μg/kg


Liver




30 μg/kg


Kidney




10 μg/kg


Muscle’


























B.


Annex II is amended as follows:






2.


Organic compounds







Pharmacologically active substance(s)


Animal species


Other provisions










‘2.75.


Alfaprostol






Bovine, porcine, equidae


 










2.76.


Cefazolin






Bovine


For intramammary use only (except if the udder maybe used as food for human consumption).










2.77.


Medroxyprogesterone acetate






Ovine


For intravaginal use for zootechnical purposes only










2.78.


Propylene glycol






All food producing species’


 


















C.


Annex III is amended as follows:






1.


Anti-infectious agents






1.2.


Antibiotics






1.2.4.


Cephalosporins










Pharmacologically active substance


Marker residue


Animal species


MRLs


Target tissues


Other provisions










‘1.2.4.2.


Cephapirin






Sum of cephapirin and desacetylcephapirin


Bovine


100 μg/kg


Kidney


Provisional MRLs expire on 1. 1. 1999




50 μg/kg


Muscle, liver, fat




10 μg/kg


Milk’


























D.


Annex IV is amended as follows:
List of pharmacologically active substances for which no maximum levels can be fixed:






‘9.


Chloroform’