Health Legislation

The decree establishes the pharmaceutical policy in Burkina Faso. The Pharmaceutical Policy is a national planning framework that expresses the government's vision, goals, objectives and strategic interventions for the development of the pharmaceutical sector. The policy aims to improve access to quality healthcare products, available throughout the country at a cost adapted to the population's purchasing power.

This document provides for standard treatment guidelines and the essential medicines list.

This decree, taken in application of the provisions of Law No. 020/2005 of January 3, 2006 and of Article 95 of Ordinance No. 1/95 of January 14, 1995, sets out the attributions and organization of regional hospital centers.

This Act provides for partnerships between the public sector and private sector for the supply of infrastructure and delivery of services as means of contributing towards sustaining economic growth, social development and infrastructure development; provides for the development and implementation of public-private partnership arrangements in Malawi for the delivery of infrastructure and services; provides for the establishment of the Public Private Partnership Commission; provides for private sector participation in state-owned enterprises, commercial entities and commercial assets, and provides for matters connected with or incidental to the foregoing.

The decree revises Niger's national list of essential medicines from 2009

This document provides a Sanitary Map of Sao Tome and Principe with the aim of achieving an efficient and equitable supply of health care.

This Act provides for the establishment of an independent Drug and Food Control Authority in South Sudan and provide an appropriate and effective independent regulatory mechanism to control and regulate the manufacture, supply, promotion, marketing, advertising, distribution and use of drugs, poisons, chemicals, cosmetics medical devices and food for human or animal use.

The document establishes the principles, norms and standards for the organization of the health care sector in Gabon.

The Health Institutions and Facilities Act of 2011 provides for a Health Facilities Regulatory Agency to license facilities for the provision of public and private health care services, establishes the Mortuaries and Funeral Facilities Agency to control and regulate facilities connected with the storage and disposal of human remains, establishes an Ambulance Council to regulate the operation of ambulance services in the country in accordance with policy standards and to provide for related matters.

This document provides a comprehensive framework for the delivery of essential primary care services and medicines through the community health system.

The Law establishes provisions relating to the hospital reform and applies to all hospital establishments in Madagascar.

This Act regulates the conduct of clinical trials for medicinal products in Mauritius.

The Decree establishes the General Bases of the National Pharmaceutical Policy.

The Kenya National Guidelines for the Implementation of the Basic Care Package offer a structured approach to delivering essential health services to vulnerable populations, focusing on comprehensive care, prevention, and treatment to improve overall health outcomes.

The Kenya National Infection Prevention and Control Guidelines for Health Services (2010) provide essential protocols and best practices to prevent and control infections in healthcare settings, ensuring the safety of patients, staff, and the community.

This Law defines the legal provisions relating to medicines, medical devices, other health products and the practice of pharmacy in the Islamic Republic of Mauritania. This Law is published in a collection of other legislative acts and can be found on page 3 of the file.

The Diploma approves the Medicines Registration Manual. The purpose of the Manual is to (a) Standardize the procedures and activities relating to the registration of medicines; (b) Clarify the doubts that professionals have encountered when interpreting the Registration Regulations; (c) Support professionals in the field in carrying out their daily activities in a standardized way; (d) Support applicants in complying with registration and post-registration procedures; (e) to make the registration process an optimized and increasingly swift process. 

The purpose of the Regulation is to define the procedures for approving pharmaceutical products for human use in the member states of the West African Economic and Monetary Union.

This decree regulates the conditions for the creation and opening of all private health establishments offering reproductive health care and services.

The Decree sets out the conditions for manufacturing and importing contraceptive products into Burkina Faso.