Guidelines for Medical Devices Registration - Sierra Leone
(2013; 11 pages)


The purpose of Drug Registration is to ensure that a pharmaceutical product has been adequately tested and evaluated for safety, efficacy and quality, and that the product information provided by the manufacturer is accurate. It also allows the pharmaceutical product to be placed on the market until the registration period for the product has expired.

The Pharmacy Board of Sierra Leone has developed and adopted the following guidelines: Guidelines for the registration of Medical Devices.

These guidelines are intended to facilitate the registration process of Medical Devices, and are meant to be adopted and implemented by all stakeholders intending to market Medical Devices in Sierra Leone.

The overall goal of these guidelines is to achieve the highest practicable standards of the quality of products imported into Sierra Leone and in addition to ensure the safety, quality and efficacy for these products( medical devices) manufactured, imported, exported and distributed to ensure the protection of the public health as envisaged by the Pharmacy and Drugs Act.

It should be noted however, that these guidelines are subject to review as and when necessary by the Pharmacy Board of Sierra Leone.

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