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Drug Act B.E. 2510 (A.C. 1967).

País/Territorio
Tailandia
Tipo de documento
Legislación
Fecha
1967
Fuente
FAO, FAOLEX
Materia
Ganado
Palabra clave
Medicamentos Sanidad animal Autorización/permiso Higiene/procedimientos sanitarios Registro Comercio internacional Inspección
Área geográphica
Asia, Asia y Pacifico, Mares del Asia Oriental, Océano Índico, Asia Sudoriental
Entry into force notes
This Act enters into force 60 days after its publication in the Government Gazette.
Resumen

This Act prescribes provisions for the issuance of licences to produce or sell drugs. A Drug Board shall be appointed and shall have duties specified in Chapter I. Chapters II to VI deal with matters related to the application for and issuance of licences concerning modern and traditional drugs and duties of the licensee when producing, selling or importing such drugs. It shall be prohibited to produce, sell or import fake drugs, sub-standard drugs or deteriorated drugs as specifies in Chapter VIII. The Minister is empowered to give notice in the Government Gazette of pharmacopoeias, substances which are drugs, dangerous drugs, specially controlled drugs, common household drugs, etc. (Chapter IX). Any person licensed to produce or import drugs is required to apply to the competent officer for registration of the drug formula (Chapter X). Competent officers in the performance of their duties enter upon the premises for the production, sale, importation or storage of drugs during working hours to inspect compliance with this Act. Chapter XIII establish provisions on the suspension and revocation of a licence.

Texto completo
Inglés

Referencias - Legislación

Enmendado porr

Drug Act (No.5) B.E. 2530.

Legislación | Tailandia | 1986

Palabra clave: Medicamentos, Autorización/permiso, Sanidad animal, Higiene/procedimientos sanitarios, Inspección, Comercio internacional, Infracciones/sanciones

Fuente: FAO, FAOLEX