Home Category Region Publishers About Us Contact Us
Japanese Korean Chinese
Home > Market Research Report > Pharmaceutical > The Regulatory Environment for Pharmaceutical Products and Medical Devices in Key Sub-Saharan African Countries
Category
Pharmaceutical (4989)
Bone Disease Treatment (46)
Cancer (883)
Diabetes (159)
Drug Delivery System (184)
Drug Discovery (1403)
Generic Drugs (128)
Infectious Disease (406)
Mental Disease (98)
Neurodegenerative Disease (180)
Obesity Treatment (49)
OTC Drug (149)
Pharmaceutical Companies (562)
Prescription Drugs (120)
Regulation (122)
Vaccines (178)
Veterinary Medicine (28)
Market Research Report

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

Published by Frost & Sullivan
Published July, 2007 Product code 53783
Content info 190 Pages
Price
US $ 6000 Web Access (Regional License)
US $ 6500 Hard Copy & Web Access (Regional License)


The Regulatory Environment for Pharmaceutical Products and Medical Devices in Key Sub-Saharan African Countries published by Frost & Sullivan in July, 2007. This report consists of 190 Pages and the price starts from US $ 6000.

Introduction

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
Back to Top