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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”.

Country/Territory
Armenia
Document type
Regulation
Date
2018
Source
FAO, FAOLEX
Subject
Livestock, Food & nutrition
Keyword
Public health MRL-maximum residue limit Inspection Food quality control/food safety Drugs
Geographical area
Asia, CIS (Commonwealth of Independent States), Europe, Europe and Central Asia, Landlocked Developing Nations, Western Asia
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.
Abstract

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).

Full text
Russian
Website
www.globus.ru