3Directive 2001/82/EC ,On the Community code relating to veterinary medicinal products[S].
4Regulation (EC) No 470/2009 ,Laying down Community procedures for the establishment of residue bruits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/ 2004 of the European Parhament and of the Council[S].
5Commission Regulation (EU) No 37/2010, On pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin[S].
6Council Directive 96/22/EC, Concerning the prohibition on the use in stockfarming of certain substances having a hormonal or thyrostatic action and of β-agonists, and repealing Directives 81/602/EEC, 88/ 146/EEC and 88/299/EEC[S],.
7Council Decision 1999/879/EC ,Concerning the placing on the market and administration of bovine somatotrophin (BST) and repealing Decision 90/218/EEC[S].
8Council Directive 96/23/EC,On measures to monitor certain substances and residues thereof in hve animals and animal products and repealing Directives 85/358/EEC and 86/469/EEC and Decisions 89/187/EEC and 91/664/EEC[S].
9U.S. Food and Drug Administration. 21CFR556,Tolerances for residues of new animal drugs in food[S].
10U.S. Food and Drug Administration. 21CFR530.41 ,Drugs prohibited for extralabel use in animals[S].
