This Regulation, based on the provisions of the Montenegrin Veterinary Law, prescribes the maximum permitted quantities or levels of residues of pharmacologically active substances of veterinary medicinal products in excretions and body fluids of live animals, organs and tissues of slaughtered animals and products of animal origin (detail laid down in Annex 1). This text also transposes the requirements contained in the Commission Regulation (EU) No. 914/2010 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance sodium salicylate.