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Décret No 2023-422 portant approbation des status modifiés de l'Agence béninoise de Régulation pharmaceutique désormais dénommée Agence béninoise du Médicament et des autres produits de Santé
This Decree approves the amended statutes of the Beninese pharmaceutical regulatory agency, now named “Beninese Agency for Medicines and other Health Products”.
Décret No 2022-915/PRN/MSP/P/AS du 30 novembre 2022, portant approbation des statuts de l'Agence Nigérienne de Règlementation du secteur Pharmaceutique
The Decree sets out the statutes of the Nigerian Pharmaceutical Regulatory Agency.
Standards Treatment Guidelines Pediatrics (Volume 2)
The document establishes the Paediatrics treatment guidelines in Rwanda.
Décret No 2022-824 portant création et fixant les règles d'organisation et de fonctionnement de l'Agence sénégalaise de Réglementation pharmaceutique
This Decree establishes and fixes the rules of organization and operation of the Senegalese Pharmaceutical Regulatory Agency (ARP)
Décret No 100/039 du 26 février 2021 portant création, organisation et fonctionnement de l'Autorité burundaise de régulation des médicaments a usage humain et des aliments, "ABREMA" en single
The law creates the Burundian Authority for the Regulation of Medicines for Human Use and Food. The authority's general aim is to protect public health by promoting the quality and safety of products such as prefabricated and ambient foods, medicines for human use, cosmetics and dietary products containing active ingredients, herbal medicines, traditional medicines, and medical devices, among others.
Drugs and Related Products Registration Regulations
The Regulation sets up rules in the registration of drugs and related products manufactured, imported, exported, advertised, sold, distributed or used in Nigeria.
Standard treatment guidelines and national essential medicines list for Tanzania Mainland
These 2021 Guidelines (sixth edition) establish the protocols for standard treatment in Tanzania as well as the National Essential Medicines List.
Specifications for Essential Medicines Supplies
Specifications for essential medicines supplies.
Decreto No 115/2020 Aprova o Estatuto Orgânico da Autoridade Nacional Reguladora de Medicamento
The Decree approves the Organic Statute of the Autoridade Nacional Reguladora de Medicamento (The National Medicines Regulatory Authority). The purpose of this Decree is to define the rules governing the organization, management and operation, as well as the powers of its bodies.
Guidelines to operate a private Emergency Medical Services or private ambulance services
The Guidelines provide requirements to provide private emergency medical services or private ambulance services in Rwanda.
Medicines and related substances regulations
These Regulations provide rules on the registration and access to the market to medicine; licensing requirements for pharmaceutical operations, manufacturers, wholesalers and dispensaries; as well as on record-keeping, import of medicines, and clinical trials, etc.
Pharmacy and Medicines Regulatory Authority Act
This Act establishes the Pharmacy and Medicines Regulatory Authority; provides for the functions and powers of the Authority; and provides for matters connected therewith and incidental thereto.
Loi N° 2017-541 du 3 août 2017 relative à la régulation du secteur pharmaceutique
The objective of the law is to establish an institutional framework for regulating the pharmaceutical sector to ensure market approval and use of pharmaceutical products that are accessible, safe, efficient, and of appropriate quality (art.2). It notably establishes the Authority for pharmaceutical regulation (Autorité Ivoirienne de Regulation Pharmaceutique - AIRP) and addresses its mandates (chapter 1).
Lei No 12/2017 Lei de medicamento, vacinas e outros produtos biológicos para o uso humano
This Law establishes the rules for the efficient and safe production, distribution, use and availability, as well as quality assurance of medicines, vaccines, biological and health products for citizens.
The National Medical Supplies Agency Act
This Act repeals and replaces the National Pharmaceutical Procurement Unit Act, 2012 to establish the National Medical Supplies Agency as a public service agency responsible for the procurement, warehousing and distribution of drugs and medical supplies in a transparent and cost-effective manner for and on behalf of all public institutions throughout Sierra Leone.
Medicines and Related Substances Control Act, 2015
This Act provides for the establishment of a Medicines Regulatory Authority; for the registration of medicines and medical devices; for the control of medicines and scheduled substances, and for incidental matters.
Basic Paediatric Protocols
This pocket book consists of guidelines on the classification of illness severity, criteria for admission, and inpatient management of the major causes of childhood mortality such as pneumonia, diarrhea, malaria, severe malnutrition, meningitis, HIV and neonatal conditions. The guidelines target the management of the seriously ill newborn or child in the first 24 - 48 hours of arrival at the hospital.
Procedures for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products
These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.
Nigeria Standard treatment guidelines (2nd Edition)
The document provides the guideline treatment and the standard of care for the Nigerian Population. Taking also into consideration different approaches from the health sector.
Lignes directrices sur l’approvisionnement en médicaments essentiels en République Démocratique du Congo
This document provides guidelines on the supply of essential medicines in the Democratic Republic of Congo.