Cabinet Regulation No. 401 of 2004 on Procedures for Monitoring of Adverse Reactions Caused by Veterinary Medicinal Products País/Territorio Letonia Tipo de documento Reglamento Fecha 2007 (2008) Fuente FAO, FAOLEX Fuente original Latvijas Vēstnesis, 61 (3637), 13.04.2007. Materia Ganado Palabra clave Sanidad animal Medicamentos Cuestiones de procedimiento Alimentos para animales/piensos Envasado/etiquetado Normas sobre calidad ambiental Protección del medio ambiente Normas Área geográphica Europa, Europa y Central Asia, Países de la Unión Europea, Europa Septentrional Resumen These Regulations prescribe the procedures by which the monitoring of possible adverse reactions caused by veterinary medicinal products shall be performed. These Regulations apply to the adverse reactions caused to animals - by the use of veterinary medicinal products (also medical treatment pre-mixture added to medicated feed); by the medicinal products, which are intended for humans, used in veterinary medicine; and by the use of veterinary medicinal products in a manner incompatible with the information indicated on a labelling and package leaflet; humans - by the incidental use of veterinary medicinal products or their use for animals; possible - by the veterinary medicinal products getting into the environment (pollution); by the inefficiency of veterinary medicinal products; and by the changes during withdrawal period of the veterinary medicinal products from the organism. Texto completo Letón/Inglés Página web likumi.lv Referencias - Legislación Implementa 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