Commission Regulation (EC) No 613/98 of 18 March 1998 amending Annexes 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 (Text with EEA relevance)
Commission Regulation (EC) No 613/98of 18 March 1998amending Annexes 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(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 originOJ L 224, 18. 8. 1990, p. 1., as last amended by Commission Regulation (EC) No 426/98OJ L 53, 24. 2. 1998, p. 3. and in particular Articles 6 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 potassium nitrate, potassium dl-aspartate, potassium glucuronate and potassium glycerophosphate should be inserted into Annex II to Regulation (EEC) No 2377/90;Whereas, in order to allow for the completion of scientific studies, florfenicol and moxidectin should be inserted into Annex III to Regulation (EEC) No 2377/90;Whereas, in order to allow for the completion of scientific studies, the duration of the validity of the provisional maximum residue limits previously defined in Annex III of Regulation (EEC) No 2377/90 should be extended for albendazole sulphoxide and carprofen;Whereas it appears that maximum residue limits cannot be established for metronidazole because residues, at whatever limit, in foodstuffs of animal origin might constitute a hazard to the health of the consumer, whereas it should 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 /EECOJ L 317, 6. 11. 1981, p. 1., as last amended by Directive 93/40/EECOJ L 214, 24. 8. 1993, p. 31. 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 THIS REGULATION:
Article 1Annexes II, III and IV of Regulation (EEC) No 2377/90 are hereby amended as set out in the Annex hereto.
Article 2This Regulation shall enter into force on the 60th 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, 18 March 1998.For the CommissionMartin BangemannMember of the CommissionANNEXA.Annex II is modified as follows:1.Inorganic chemicals
Pharmacologically active substances(s)Animal speciesOther provisions
"Potassium nitrateAll food producing species
Potassium DL-aspartateAll food producing species
Potassium glucuronateAll food producing species
Potassium glycerophosphateAll food producing species"
B.Annex III is modified as follows:1.Anti-infectious agents1.2.Antibiotics1.2.11.Florfenicol and related compounds
Pharmacologically active substanceMarker residueAnimal speciesMRLsTarget tissuesOther provisions
"FlorfenicolSum of florfenicol and its metabolites measured as florfenicol-amineFish1000 µg/kgMuscle and skin in natural proportionsProvisional MRLs expire on 1.7.2001"
2.Antiparasitic agents2.1.Agents acting against endoparasites2.1.1.Benzimidazoles and pro-benzimidazoles
Pharmacologically active substanceMarker residueAnimal speciesMRLsTarget tissuesOther provisions
"Albendazole sulphoxideSum of albendazole, albendazole sulphoxide, albendazole sulphone and albendazole 2-amino sulphone, expressed as albendazoleBovine, ovine, pheasant1000 µg/kgLiverProvisional MRLs expire on 1.1.2000"
500 µg/kgKidney
100 µg/kgMuscle, fat
Bovine, ovine100 µg/kgMilk
2.3.Agents acting against endo- and ectoparasites2.3.1.Avermectins
Pharmacologically active substanceMarker residueAnimal speciesMRLsTarget tissuesOther provisions
"MoxidectinMoxidectinEquidae50 µg/kgMuscleProvisional MRLs expire on 1.1.2000"
500 µg/kgFat
100 µg/kgLiver
50 µg/kgkidney
4.Anti-inflammatory agents4.1.Nonsteroidal anti-inflammatory agents4.1.1.Arylpropionic acid derivative
Pharmacologically active substanceMarker residueAnimal speciesMRLsTarget tissuesOther provisions
"CarprofenCarprofenBovine1000 µg/kgLiver, kidneyProvisional MRLs expire on 1.1.2000"
500 µg/kgMuscle, fat
Equidae1000 µg/kgLiver, kidney
50 µg/kgMuscle
100 µg/kgFat
C.Annex IV is modified as follows:List of pharmacologically active substances for which no maximum levels can be fixed"Metronidazole."