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Décision No 0118/D/MINSANTE/CAB fixant les prix et les modalités de mise à disposition des kits de diagnostic rapide du paludisme au Cameroun
This decision by the minister of public health provides the prices and conditions of availability of rapid malaria diagnosis kits.
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.
Mental Health Act, 2012 Act 846
The Mental Health Act of 2012 provides for mental health care and for related matters. Among other things, it establishes a Mental Health Authority (sections 1 to 23), enshrines a set of rights for persons with mental disorder (sections 54 to 63), and establishes a mental health fund (sections 80 to 87).
Guidelines for prevention of mother to child transmission of HIV/AIDS in Kenya 4th edition
The Revised Guidelines (4th edition) for Prevention of Mother-to-Child Transmission (PMTCT) of HIV and AIDS provide more detailed and effective interventions to reduce the risk of mother-to-child transmission (MTCT) than previous editions. They emphasize the early initiation of ARV prophylaxis starting at 14 weeks, highlighting the importance of early antenatal care (ANC) attendance for all women.
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.
Guidelines for antiretroviral therapy in Kenya
These guidelines outline standardized protocols for the initiation and management of HIV treatment, emphasizing early treatment initiation and adherence to improve health outcomes. They incorporate recommendations for monitoring treatment efficacy, managing side effects, and addressing co-infections, ensuring a patient-centered approach in diverse healthcare settings.
Clinical Trials Act
This Act regulates the conduct of clinical trials for medicinal products in Mauritius.
Loi No 2011-16, portant création d’un Etablissement Public à caractère administratif dénommé « Centre National de Lutte contre le Cancer"
The law creates a public administrative establishment, with legal personality and financial autonomy, called the Centre national de lutte contre le cancer (National Cancer Center).
Decreto presidencial No 180/10 as bases gerais da política nacional farmacêutica
The Decree establishes the General Bases of the National Pharmaceutical Policy.
Loi n° 040 -2010/an portant lutte contre le tabac au Burkina Faso
The law reinforces the fight against the use and consumption of tobacco and tobacco products in Burkina Faso. The scope of the law covers the industrial or supervised cultivation of tobacco, the manufacture, packaging, marketing and consumption of tobacco and tobacco products, and exposure to tobacco smoke.
National Guidelines for HIV testing and counselling in Kenya
These Guidelines outline standardized protocols for voluntary testing and counselling to enhance access to HIV services, ensure informed consent, and promote client confidentiality and support.
National Quality Management Guidance Framework for HIV Testing and Counseling in Kenya
This Guidance Framework outlines strategies and standards to ensure high-quality, client-centered HIV testing and counselling services, promoting accuracy, safety, and confidentiality in the process.
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.
Ordonnance 056/2009/PRG/SGG relative à la Prevention, Prise en charge et le Contrôle du VIH/sida
The law regulates the management and control of HIV/AIDS in the Republic of Guinea.