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

País/Territorio
Chipre
Tipo de documento
Legislación
Fecha
2006 (2011)
Fuente
FAO, FAOLEX
Fuente original
Official Gazette of Cyprus Republic no. 4069 of 2006, Appendix I.
Materia
Ganado
Palabra clave
Alimentos para animales/piensos Sanidad animal Producción animal Autorización/permiso Legislación básica Biotecnología Negocios/industria/corporaciones Clasificación/declasificación Plagas/enfermedades Hormonas/esteroides Inspección Institución Derechos de propiedad intelectual/patentes Comercio interior Comercio internacional Envasado/etiquetado Procedimientos judiciales/procedimientos administrativos Toxicidad/envenenamiento Protección del medio ambiente Salud pública Investigación Evaluación/manejo de riesgos Roedores Normas Medicamentos
Área geográphica
Asia, Europa, Europa y Central Asia, Países de la Unión Europea, Mediterráneo, Medio Oriente, Asia Occidental
Resumen

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.

Texto completo
Griego
Página web
www.mof.gov.cy

Referencias - Legislación

Implementa

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.

Legislación | Unión Europea | 2006

Palabra clave: Sanidad animal, Medicamentos

Fuente: FAO, FAOLEX

Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products.

Legislación | Unión Europea | 2001

Palabra clave: Legislación básica, Sanidad animal, Medicamentos, Autorización/permiso, Recopilación de datos/informes, Acceso-a-la-información, Inspección, Comercio interior, Comercio internacional, Infracciones/sanciones

Fuente: FAO, FAOLEX