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The Pharmaceutical and Poisons Amendment Law no. 67 of 2019.

País/Territorio
Chipre
Tipo de documento
Legislación
Fecha
2019
Fuente
FAO, FAOLEX
Fuente original
Official Gazette of Cyprus Republic no. 4704 of 2019, Appendix I.
Materia
Desechos y sustancias peligrosas, General
Palabra clave
Autorización/permiso Clasificación/declasificación Recopilación de datos/informes Cumplimiento/aplicación Higiene/procedimientos sanitarios Toxicidad/envenenamiento Salud pública Relaciones internacionales/cooperación Envasado/etiquetado
Área geográphica
Asia, Europa, Europa y Central Asia, Países de la Unión Europea, Mediterráneo, Medio Oriente, Asia Occidental
Resumen

This Law, consisting of 12 articles and amending the 1959 version of the Pharmacy and Poisons Law and its subsequent versions, provides for the modernisation and adaptation of the pharmaceutical practice to the necessary reforms in view of the implementation of the General Health System and implements the Regulation (EC) No. 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency. The following relevant terms are defined: disability; generic medicinal product; dosage of medicinal product; active substance; recipient; prescription execution; controlled drug; outpatient; recurring prescription; validating decree; non-prescription medicinal products; healthcare service; pharmaceutical product. The Law defines that pharmacists may execute prescriptions and sell or supply pharmaceutical products; specifies conditions for establish a hospital pharmacy in a hospital; prescribes conditions for the implementation of medical recipes, the supply of pharmaceutical products and active substances and excipients; details duties of pharmacists concerning prescription files, pharmaceutical products containing controlled drugs in accordance with the provisions of the World Health Organisation. The Law provides for a non-exhaustive list of information that medical prescription must include.

Texto completo
Griego
Página web
www.mof.gov.cy

Referencias - Legislación

Implementa

Regulation (EC) No. 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency.

Legislación | Unión Europea | 2004

Palabra clave: Medicamentos, Institución, Autorización/permiso, Infracciones/sanciones, Sanidad animal

Fuente: FAO, FAOLEX

Enmienda

The Pharmacy and Poisons Law. Chapter 254 of the Laws.

Legislación | Chipre | 1947 (2022)

Palabra clave: Toxicidad/envenenamiento, Venta, Sanidad animal, Medicamentos, Autorización/permiso, Negocios/industria/corporaciones, Clasificación/declasificación, Sustancias peligrosas, Inspección, Comercio interior, Envasado/etiquetado, Entidad no gubernamental, Infracciones/sanciones, Cuestiones de procedimiento, Salud pública, Registro, Normas

Fuente: FAO, FAOLEX