ker je treba po znanstveni presoji, ki jo opravi Odbor za zdravila za uporabo v veterinarski medicini, sprejeti najvišje dovoljene količine zaostankov po hitrem postopku, ki zagotavlja tesno sodelovanje med Komisijo in državami članicami v odboru, ustanovljenim na podlagi Direktive Sveta 81/852/EGS z dne 28. septembra 1981 o približevanju zakonodaj držav članic v zvezi z analiznimi, farmako-toksikološkimi in kliničnimi standardi ter protokoli za preskušanje zdravil za uporabo v veterinarski medicini fn, kakor je bila nazadnje spremenjena z Direktivo 87/20/EGS fn;
Whereas, after scientific assessment by the Committee for Veterinary Medicinal Products, maximum residue levels must be adopted by a rapid procedure which ensures close cooperation between the Commission and the Member States through the Committee set up under Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products (4), as last amended by Directive 87/20/EEC (5);