Regulation of Medical Devices: A Step-by-step Guide. (WHO Regional Publications, Eastern Mediterranean Series 38)
(2016; 65 pages) [French]


The purpose of Regulation of medical devices: a step-by-step guide is to improve access by countries to quality and safe medical devices by offering guidance on strengthening their regulatory controls. It provides decision-makers with a roadmap for implementing regulatory systems in their national settings and a step-by-step approach towards the development of national programmes for the regulation of medical devices. It can be applied by any country seeking to develop its regulatory capacity.

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