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”.

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).