National Medicines Regulatory Authority Act, No. 5 of 2015. (Published as a Supplement to Part II of the Gazette of the Democratic Socialist Republic of Sri Lanka of March 20, 2015)
(2015; 98 pages)

Resumen

An act to provide for the establishment of a regulatory authority to be known as the National Medicines Regulatory Authority which shall be responsible for the regulation and control of registration, licensing, manufacture, importation and all other aspects pertaining to medicines, medical devices, borderline products and for the conducting of clinical trials in a manner compatible with the national medicines policy; to provide for the establishment of divisions of the National Medicines Regulatory Authority including the medicines Regulatory Division, Medical Devices Regulatory Division, borderline products Regulatory Division and Clinical Trials Regulatory Division; to establish a National Advisory Body; to repeal the Cosmetics, Devices and Drug Act, No. 27 of 1980; and for matters connected therewith or incidental thereto.

Documentos relacionados
 
El Portal de Información - Medicamentos Esenciales y Productos de Salud de la OMS fue diseñado y es mantenido por la ONG Human Info. Última actualización: le 1 diciembre 2019