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Ministerial Decree No. 380 validating the Regulation on drug safety requirements.

País/Territorio
Kazajstán
Tipo de documento
Reglamento
Fecha
2008
Fuente
FAO, FAOLEX
Materia
Ganado
Palabra clave
Medicamentos Certificación Sanidad animal
Área geográphica
Mar Aral, Asia, Mar Caspio, Asia Central, CEI (Comunidad de Estados Independientes), Europa y Central Asia, Naciones en desarrollo sin litoral, Asia del Norte
Resumen

This Ministerial Decree establishes the safety requirements for drugs and biological preparations used for veterinary purposes, including those manufactured on or imported into the country. Such drugs shall be authorized for manufacture and application only following state registration. This Ministerial Decree shall not apply to experimental drugs, samples imported for state registration and preparations containing GMOs. Mandatory radiation control and eradication of toxic substances, toxic and infected plants shall be carried out at the preliminary stage of procurement of raw materials for the manufacture of drugs and biological preparations. All substances and packaging materials used in the manufacture of drugs and biological preparations shall be certified. Drugs shall be manufactured from medicinal substances registered in Kazakhstan.

Texto completo
Ruso
Página web
www.government.kz