The Regulatory Environment for Pharmaceutical Products and Medical Devices in Key Sub-Saharan African Countries

Abstract

Research was carried out on the regulatory environment for pharmaceutical products and medical devices in eight key sub-Saharan African countries, namely Botswana, Kenya, Namibia, Nigeria, South Africa, Tanzania, Uganda and Zambia. The legislation and processes involved in the registration, import and distribution of pharmaceutical products and medical devices were analysed. A comprehensive decision support database with core health indicators for 8 sub-Saharan African countries is also provided.