Health Legislation

The document establishes the list of essential medicines in the Republic of Guinea.

The document provides the national list of essential medicines from 2016.

These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.

The diploma approves the National List of Essential Medicines. It is a mandatory tool for Health Professionals to use throughout the process of searching for, acquiring, distributing and prescribing medicines within the National Health Service.

The Namibia Essential Medicines List acts as a guide for the level of availability and use of essential medicines based on the skills levels of health workers as well as the availability of diagnostic facilities at the various levels of the Namibian public sector healthcare system.

This Ministerial Decree regulates information and advertising of medicines and other health products.

This document provides guidelines on the supply of essential medicines in the Democratic Republic of Congo.

This Ministerial decree regulates the trade of pharmaceutical products in the Democratic Republic of the Congo.

This Regulation is to determine the fee payable for registration and license of food, medicine, health professional and health institutions.

This document establishes the National List of Essential Medicines for Paediatrics to enable the availability, accessibility and affordability of quality and safe health products and ensure their rational use.

This document establishes the National Essential Medicine List for Adults to enable the availability, accessibility and affordability of quality and safe health products and ensure their rational use.

The document provides the 7th version of the essential medicines list and standard treatment guidelines for Zimbabwe.

This regulation is issued to implement the Food Medicine and Health Care Administration and Control Proclamation No 661/2009. and covers among other aspects of food safety and quality which includes manufacturing, storage and transportation among other aspects; sale of alcohol; medicine administration and control which includes manufacturing, registration, storage, transportation, importation ad clinical trials among others; traditional and complementary medicine administration and control; post-marketing surveillance; control of tobacco products and places prohibited for smoking among other aspects.  

The Act regulates the quality and safety of medicines and related products and connected matters.

This Act promotes and protects the health and safety of the general public through safeguarding, maintaining and enforcing the highest standards in the practice of pharmacy.

The decree creates a multi-sectoral committee to combat counterfeiting and the illicit sale of medicines and other pharmaceutical products, reporting to Niger's Minister of Public Health.

These Regulations govern the issuance of licenses for the importation, exportation, manufacture, distribution, and retail of drugs, etc.

The Public Health Act repeals, re-enacts, consolidates and amends the law relating to public health in Botswana.

This Act provides for the registration, regulation of the sale, distribution, importation, exportation, manufacture and dispensing of medicines and related substances, and matters incidental thereto.

This Act makes provisions for the establishment of the Kenya Medical Supplies Authority and for connected purposes.