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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”.

País/Territorio
Armenia
Tipo de documento
Reglamento
Fecha
2018
Fuente
FAO, FAOLEX
Materia
Ganado, Alimentación y nutrición
Palabra clave
Salud pública Límite máximo de residuos Inspección Control de calidad de los alimentos/inocuidad de los alimentos Medicamentos
Área geográphica
Asia, CEI (Comunidad de Estados Independientes), Europa, Europa y Central Asia, Naciones en desarrollo sin litoral, Asia Occidental
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.
Resumen

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).

Texto completo
Ruso
Página web
www.globus.ru