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Medicines and related substances Act
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.
The Kenya Medical Supplies Authority Act
This Act makes provisions for the establishment of the Kenya Medical Supplies Authority and for connected purposes.
Arrêté No 69/MSP/DGSP/DPHLMT, portant création du Comité d’Experts chargé de l’évaluation technique des dossiers de demande d’homologation des produits pharmaceutiques à usage humain
The decree establishes a Committee of Experts in charge of technical evaluation, whose mission is to carry out the technical evaluation of applications for registration of pharmaceutical products for human use. It also gives an opinion on the quality, safety and efficacy of pharmaceutical products for human use submitted for registration.
Arrêté No 68/MSP/DGSP/DPHLMT, portant création de la Commission Nationale du Médicament (CNM)
The decree creates the Commission Nationale du Médicament (CNM) for human use, whose mission is to validate the work of the Expert Committee responsible for the technical evaluation of applications for marketing authorization for pharmaceutical products for human use. It also gives a final opinion on marketing authorization applications; applications for renewal, extension of variation and transfer of marketing authorization; temporary suspension of marketing authorization; and proposals for definitive withdrawal of marketing authorization.
Essential drug list
These guidelines establish an Essential Drug List of Botswana of 2012 and provide the requirements regarding the levels of availability across health care providers.
Décret n°2012-966/PRES/PM/MS/MEF/MICA/MRSI portant adoption d'une politique pharmaceutique 2012-2016
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.
Standard Treatment Guidelines and Essential Medicines List of Common Medical Conditions in the Kingdom of Swaziland
This document provides for standard treatment guidelines and the essential medicines list.
Arrêté No 466/MSP/DGSP/DPHL/MT, portant additif à l’arrêté n° 065/MSP/DGSP/DPHL/MT du 09 février 2009 portant Liste Nationale des Médicaments essentiels (LNME)
The decree revises Niger's national list of essential medicines from 2009
Drug and Food Control Authority Act, No 37
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.
Décret exécutif No 11-122 du 15 Rabie Ethani 1432 portant statut particulier des fonctionnaires appartenant au corps des sage-femmes de santé publique
The Decree N°11-122 addresses the special status of civil servants belonging to the corps of public health midwives. It was published in the Official Journal of 20 March 2011 (pages 36 - 40)
Clinical Trials Act
This Act regulates the conduct of clinical trials for medicinal products in Mauritius.
Ministerial Order no 20/23 determining the code of professional conduct of Nurses and Midwives
The Order establishes the professional Code of conduct for nurses and midwives in Rwanda. This Order concerns nurses and midwives registered with the National Council of Nurses and Midwives.
Decreto presidencial No 180/10 as bases gerais da política nacional farmacêutica
The Decree establishes the General Bases of the National Pharmaceutical Policy.
Loi No 2010-022 du 10 février 2010 relative a la pharmacie
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.
Diploma Ministerial No 223/2010 Aprova o Manual de Registo de Medicamentos
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.
Règlement No 06/2010/CM/UEMOA relatif aux procédures d’homologation des produits pharmaceutiques à usage humain
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.
Minimum Standards for Courses of Study for the Bachelor of Nursing Science Program
This document sets out the minimum standards for courses and the curricula for the Bachelor of Nursing Science Program in Uganda.
The Nursing and Midwifery Act
This Act makes provisions for the protection, promotion and preservation of public health, safety and welfare through regulation and control of nursing and midwifery education and practice.
Décret n° 2009-720/PRES/PM/MS/MEF/MCPEA portant conditions de fabrication et d'importation des produits contraceptifs au Burkina Faso
The Decree sets out the conditions for manufacturing and importing contraceptive products into Burkina Faso.
Liste Nationale des médicaments essentiels en République Centrafricaine
This document establishes a National List of Essential Medicines in the Central African Republic.