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.
Table of Contents
- Executive Summary
- Research Scope and Methodology
- Introduction and Background
- Kenya
- Nigeria
- South Africa
- Tanzania
- Botswana
- Namibia
- Uganda
- Zambia
- Decision Support Database
| 
