Law no. 10 of 2006 concerning Veterinary Medicinal Products (Quality Control, Registration, Circulation, Manufacture, Administration and Use).

Sujet

Bétail

Mot clé

Aliments pour animaux Santé des animaux Production animale Autorisation/permis Législation de base Biotechnologie Commerce/industrie/sociétés Classement/déclassement Parasites/maladies Hormones/stéroïdes Inspection Institution Droits de propriété intellectuelle/brevets Commerce intérieur Commerce international Emballage/étiquetage Procédures judiciaires/procédures administratives Toxicité/empoisonnement Protection de l’environnement Santé publique Recherche Évaluation/gestion des risques Rongeurs Normes Médicaments

Aire géographique

Asie, Europe, Europe et Asie Centrale, Pays de l'Union Européenne, Méditerranée, Moyen-Orient, Asie Occidentale

Résumé

This Law, consisting of 106 articles and divided into nine Parts, in harmonisation with the Directive 2001/82/EC of the European Parliament and of the Council on veterinary medicinal products, applies to: preparation of veterinary medicinal products, including premixes for medicated animal feed, active substances used as raw materials, specific substances that may be used as veterinary medicinal products with anabolic, anti-infectious, anti-parasitic, anti-inflammatory, hormonal or psychotropic properties, except for: inactivated or non-inactivated immunological veterinary medicinal products prepared from pathogens and antigens from an animal of a livestock and used for the treatment of the same animal, veterinary medicinal products based on radioactive isotopes. The following relevant terms are defined: adverse effects; adverse reaction in human; immunological veterinary medicinal product; galenic medicinal product; over-the-counter galenic medicinal product; dosage of veterinary medicinal product; registered; outer packaging; labelling; risks associated with the use of the product, including any risk of adverse effects on the environment and risks for human and animal health; veterinary prescription; veterinary medicinal product; distribute; retail sale; unintended use; homeopathic veterinary medicinal product; substance; manufacture of active substances used as raw materials; mixture for medicated animal feed; feed additive; serious adverse reaction; benefit/risk ratio; wholesale of veterinary medicinal products.

Texte intégral

Grec

Site web

www.mof.gov.cy

Références - Législation

Implemente

Commission Directive 2006/130/EC implementing Directive 2001/82/EC of the European Parliament and of the Council as regards the establishment of criteria for exempting certain veterinary medicinal products for food-producing animals from the requirement of a veterinary prescription.

Législation | Union européenne | 2006

Mot clé: Santé des animaux, Médicaments

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