The European medicines evaluation agency for product used in animal is EMEA-CVMP. The legal basis on three director (81/851/EEC, 81/852/EEC, 2001/82/EEC) and one regulation (2309/93/EEC).

• 欧盟的生物制品和药品统一由欧洲药品审评署(EMEA)下设的兽医药品委员会(CVMP)负责管理，三个指令(81/851/EEC、81/852/EEC和2001/82/EEC)和一个法规(2309/93/EEC)构成了管理系统的法律基础。