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Decision N 28 of the Board of the Eurasian Economic Commission “On the maximum permissible levels of residues of veterinary medicinal products (pharmacologically active substances) that may be contained in unprocessed food products of animal origin, including raw materials, and methods for their determination”.

Pays/Territoire
Arménie
Type du document
Règlement
Date
2018
Source
FAO, FAOLEX
Sujet
Bétail, Alimentation et nutrition
Mot clé
Santé publique Limite maximum de résidu Inspection Contrôle de qualité alimentaire/innocuité des produits alimentaires Médicaments
Aire géographique
Asie, CEI (Communauté des États indépendants), Europe, Europe et Asie Centrale, Nations en développement sans littoral, Asie Occidentale
Entry into force notes
This Decision enters into force after 30 calendar days after the date of its official publication, with the exception of Clause 2, which enters into force 180 calendar days after the date of its official publication.
Résumé

The Decision approves MRL of veterinary medical products that may be contained in unprocessed food products of animal origin and requires that these products be accompanied with a document indicating the veterinary medical product’s name, the date of its last use for a productive animal and the confirmation of the timing of its elimination from the body of the animal. It establishes that maximum allowable levels of veterinary drug residues (pharmacologically active substances) in non-processed food products of animal origin, including listed raw materials shall be controlled by: (a) manufacturer (supplier) of non-processed food products of animal origin, including raw materials, in the case of application of veterinary medicinal products to productive animals; (b) in the course of production control at food processing enterprises in accordance with the information provided by the manufacturer (supplier) on the use of veterinary drugs; and (c) in the course of state control (supervision).

Texte intégral
Russe
Site web
www.globus.ru