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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