Joint Ministerial Decision no. 282371 of 2006 on veterinary medicinal products. Pays/Territoire Grèce Type du document Règlement Date 2006 Source FAO, FAOLEX Source d'origine Government Gazette 731/B of 2006. Titre completJoint Ministerial Decision no. 282371 of 2006 of the Ministers of Economy and Agricultural Development and Food concerning harmonisation of the Greek legislation with the corresponding EU legislation in the field of production and circulation of veterinary medicines, in compliance with Directives 2001/82/EC and 2004/28/EC of the European Parliament and of the Council on the Community code for veterinary medicinal products. Sujet Bétail, Alimentation et nutrition, Pêche, Déchets et substances dangereuses Mot clé Santé des animaux Lait/produits laitiers Produits de la pêche Contrôle de qualité alimentaire/innocuité des produits alimentaires Viande Produits de volaille Aliments pour animaux Apiculture/sériciculture Production animale Biotechnologie Hygiène/procédures sanitaires Inspection Emballage/étiquetage Limite maximum de résidu Infractions/sanctions Parasites/maladies Protection de l’environnement Santé publique Résidus Évaluation/gestion des risques Abattage Normes Toxicité/empoisonnement Transport/dépôt Restrictions à l'utilisation Vaccination Médicaments Gestion des déchets Déchets non-ménagers Aire géographique Europe, Europe et Asie Centrale, Pays de l'Union Européenne, Méditerranée, Europe du Sud Entry into force notes June 16, 2006. Résumé This Decision, consisting of 96 articles and divided into ten Parts, establishes provisions concerning the circulation, control and manufacturing conditions of veterinary medicinal products, immunological veterinary medicinal products and homeopathic veterinary medicinal products in compliance with the mentioned Directives of the European Parliament and Council. The Decision defines the following relevant terms: veterinary medicine; substance, including: animal, vegetal, and human and chemical extracts; medicated feed; immunological veterinary medicine; homeopathic veterinary medicine; waiting time and maximum limits of residues of active substances; adverse effect; adverse effect in humans, as reaction occurring in humans after exposure to a veterinary medicine; serious side effect; periodic safety monitoring report; unauthorised use; wholesale of veterinary drugs; license holder; Organisation, as the European Medicines Agency; risk associated with the use of the product; risk benefit; veterinary prescription; primary packaging; labelling. This Ministerial Decision applies to veterinary medicines, including pre-mixtures for medicated animal feed, intended to be made available to Greek market and to active substances used as raw materials. In the case of veterinary drugs intended exclusively for aquarium fish, songbirds, homing pigeons, animals kept in terrariums, small rodents, weasels and rabbits kept exclusively as pets, this Ministerial Decision does not apply. Texte intégral Grec Site web www.e-nomothesia.gr Références - Législation Implemente Directive 2004/28/EC of the European Parliament and of the Council amending Directive 2001/82/EC on the Community code relating to veterinary medicinal products. Législation | Union européenne | 2004 Mot clé: Santé des animaux, Médicaments, Autorisation/permis, Commerce intérieur, Commerce international Source: FAO, FAOLEX Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products. Législation | Union européenne | 2001 Mot clé: Législation de base, Santé des animaux, Médicaments, Autorisation/permis, Collecte de données/déclarations, Accès-à-l'information, Inspection, Commerce intérieur, Commerce international, Infractions/sanctions Source: FAO, FAOLEX