Good Manufacturing Practice for Veterinary Medicinal Products Rules, 2018 (L.N. 3 of 2018). Country/Territory Malta Document type Regulation Date 2018 Source FAO, FAOLEX Subject Livestock Keyword Drugs Animal health Authorization/permit Inspection Geographical area Europe, Europe and Central Asia, European Union Countries, Mediterranean, Southern Europe Abstract These rules lay down the principles and guidelines of good manufacturing practice for veterinary medicinal products whose manufacture requires the authorization referred to in article 44 of Directive 2001/82/EC. Full text Spanish Website www.gov.mt References - Legislation Implements Commission Directive 91/412/EEC laying down the principles and guidelines of good manufacturing practice for veterinary medicinal products. Legislation | European Union | 1991 Keyword: Drugs, Authorization/permit, Registration, Internal trade, International trade, Animal health, Processing/handling Source: FAO, FAOLEX Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products. Legislation | European Union | 2001 Keyword: Basic legislation, Animal health, Drugs, Authorization/permit, Data collection/reporting, Access-to-information, Inspection, Internal trade, International trade, Offences/penalties Source: FAO, FAOLEX