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

Pays/Territoire
Chypre
Type du document
Législation
Date
2019
Source
FAO, FAOLEX
Source d'origine
Official Gazette of Cyprus Republic no. 4704 of 2019, Appendix I.
Sujet
Déchets et substances dangereuses, Général
Mot clé
Autorisation/permis Classement/déclassement Collecte de données/déclarations Mise en application Hygiène/procédures sanitaires Toxicité/empoisonnement Santé publique Relations internationales/coopération Emballage/étiquetage
Aire géographique
Asie, Europe, Europe et Asie Centrale, Pays de l'Union Européenne, Méditerranée, Moyen-Orient, Asie Occidentale
Résumé

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.

Texte intégral
Grec
Site web
www.mof.gov.cy

Références - Législation

Implemente

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.

Législation | Union européenne | 2004

Mot clé: Médicaments, Institution, Autorisation/permis, Infractions/sanctions, Santé des animaux

Source: FAO, FAOLEX

Amende

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

Législation | Chypre | 1947 (2022)

Mot clé: Toxicité/empoisonnement, Vente, Santé des animaux, Médicaments, Autorisation/permis, Commerce/industrie/sociétés, Classement/déclassement, Substances dangereuses, Inspection, Commerce intérieur, Emballage/étiquetage, Entité non-gouvernementale, Infractions/sanctions, Questions de procédures, Santé publique, Enregistrement, Normes

Source: FAO, FAOLEX