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Governmental Decree No. 565 On the procedure for submitting documents and information on medicinal products for veterinary use introduced into civil circulation, issuing permission to enter into civil circulation an immunobiological medicinal product for veterinary use and test reports on the compliance of batches of an immunobiological medicinal product for veterinary use with the quality indicators provided for by the regulatory document.

País/Territorio
Federación de Russia
Tipo de documento
Reglamento
Fecha
2023
Fuente
FAO, FAOLEX
Materia
Ganado
Palabra clave
Sanidad animal Medicamentos Procesamiento/manipulación Autorización/permiso Recopilación de datos/informes Acceso-a-la-información Transporte/depósito Comercio internacional Cumplimiento/aplicación
Área geográphica
Ártico, Asia y Pacifico, Mar Negro, Mar Caspio, CEI (Comunidad de Estados Independientes), Europa Oriental, Europa, Europa y Central Asia, Pacífico Norte, Pacífico Nordoeste
Entry into force notes
This Governmental Decree enters into force on 1 September 2023.
Resumen

Rules for submitting documents and information about medicinal products for veterinary use introduced into civil circulation establish the procedure for submitting to the Federal Service for Veterinary and Phytosanitary Surveillance documents and information about each batch of a medicinal product for veterinary use produced in the Russian Federation or each batch imported (transported) into the Russian Federation of a medicinal product introduced into civil circulation on the territory of the Russian Federation, with the exception of immunobiological medicinal products, by manufacturers of medicinal products and organizations importing (transporting) medicinal products into the Russian Federation. Rules for issuing a permit to put into civil circulation an immunobiological medicinal product for veterinary use establish the procedure for issuing a permit by the Federal Service for Veterinary and Phytosanitary Surveillance to put into civil circulation an immunobiological medicinal product for veterinary use manufactured in the Russian Federation or imported (transported) into the Russian Federation. Rules for issuing test reports on the compliance of batches of an immunobiological medicinal product for veterinary use with the quality indicators provided for by the regulatory document establish the procedure for issuing test reports on the compliance of batches of an immunobiological medicinal product for veterinary use with the quality indicators provided for by the regulatory document.

Texto completo
Ruso
Página web
publication.pravo.gov.ru