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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.
Lei No 22/11 Da proteção de dados pessoais
The purpose of the law is to establish the legal rules applicable to the processing of personal data with the aim of guaranteeing respect for public freedoms and the fundamental rights and guarantees of natural persons.
Data Protection Act 2011 (Act No 5 of 2012)
The Act establishes the Data Protection Commission, provide for principles for regulation of processing of personal information in order to protect and reconcile the fundamental and competing values of personal information privacy under this Act and sector-specific legislation and other related matters.
Clinical Trials Act
This Act regulates the conduct of clinical trials for medicinal products in Mauritius.
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.
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.
Food, Medicine and Health Care Administration and Control Proclamation No. 661/2009
This Proclamation regulates activities in respect of food, medicine, environmental health, health professionals, health and controllable health related institutions in the country.
Information and Communications Act
The Act provides for the re-structuring, development, and regulation of the information and communication sectors in The Gambia and for matters connected therewith.
Medicines and Related Substances Control Amendment Act
This Act amends the Medicines and Related Substances Control Act, 2003, so as to amend and delete certain definitions; provides for a period within which the Council must be appointed; provides for the appointment of chairpersons of committees established by the Council; amends provisions relating to the classification of medicines and other substances as scheduled substances; amends provisions relating to the manufacturing, packing and selling of specified Schedule 3 and specified Schedule 4 substances; deletes references to generic substitutions; substitutes references to Schedule 1, Schedule 2, Schedule 3 or Schedule 4 medicines by references to Schedule 1, Schedule 2, Schedule 3 or Schedule 4 substances; inserts provisions relating to the registration of premises engaged in the manufacturing of medicines; amends provisions relating to offences and penalties; amends provisions relating to the destruction of forfeited medicines, scheduled substances or other things; provides for the making of regulations in relation to medicines; amends provisions relating to the exclusion of medicines from the operation of the Act; amends the transitional provisions; amends provisions relating to the repeal and amendment of certain laws; and provides for matters incidental thereto.
The Pharmacy and Drugs (Amendment) Act
This Act amends section 38 of the Pharmacy and Drugs Act of 2001.
Decreto-Lei No 59/2006
This decree regulates the marketing authorization, registration, manufacture, import, export, marketing, donations and advertising of medicines for human use.
Liste nationale des médicaments essentiels par niveaux 2006
The document establishes the list of essential medicines in the Republic of Mali.
Statistics Act
This Act provides for a sustainable, effective and efficient national statistical system for The Gambia for the collection, production and dissemination of integrated, relevant, reliable, timely statistical information, establishes The Gambia Bureau of Statistics as a supervisory authority for the national statistical system.
Standard treatment guidelines and essential medicines list
The policy establishes the national list of essential medicines and treatment guidelines in Lesotho.
Ministerial Decree 12 of 2005 determining the Conditions for Opening and Operating of Wholesale Pharmaceutical Store
This Decree determines the conditions for opening and operating of wholesale pharmaceutical stores in Rwanda.
Data Protection Act
This Act establishes the framework for regulation of data protection and establishes the Data Protection Office and its mandate, etc.