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Décret No. 2023-100/PR du 11/ 10/2023 fixant les modalités du contrôle médical en assurance maladie universelle
The Decree sets out the terms and conditions of the medical inspection carried out by the Universal Health Insurance management body.
Rwanda Hospital Accreditation Standards Performance Assessment Toolkit (3rd Edition)
The Rwanda Hospital Accreditation Standards Performance Assessment Tool has been developed based on the 2nd edition of the hospital standards to assist supervisors, facility managers and staff in assessing the quality of their services. The toolkit can be used to guide the set-up of services and to improve current services. It helps to measure progress towards meeting standards and will be used by external surveyors to accredit facilities.
Rwanda Hospital Accreditation Standards 3rd Edition
The document sets accreditation standards for Hospitals in Rwanda. They are designed for use within the entire organization and cover the full range of services.
Level Two Teaching Hospital Standards
The standards define the minimum requirements that must be covered by Level Two teaching Hospitals for undergraduate and postgraduate training programs and they will be used as an inspection checklist for accreditation.
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.
Specifications for Essential Medicines Supplies
Specifications for essential medicines supplies.
Rwanda Pharmaceutical Service Accreditation Standards and Performance Assessment Toolkit
The document sets accreditation standards and a performance assessment of pharmaceutical services in Rwanda. The standards are intended for implementation within Rwandan hospitals and community pharmacies.
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.
Loi N° 2019-678 du 23 Juillet 2019 portant réforme Hospitalière
This Law aims to determine the framework for hospital reform and applies to hospitals ensuring a public service mission.
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.
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.
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.
Arrêté ministériel No 120/CAB/MIN/SP/008/CPH/OBF/2015 portant règlementation du commerce des produits pharmaceutiques en République Démocratique du Congo
This Ministerial decree regulates the trade of pharmaceutical products in the Democratic Republic of the Congo.
National Health Act
This Act provides a framework for a structured uniform health system within Namibia; consolidates the laws relating to state hospitals and state health services, and regulates the conduct of state hospitals and state health services; provides for financial assistance for special medical treatment of State patients; and provides for incidental matters.
Decreto Presidencial No 220/14 Aprova o Estatuto Orgânico do Hospital Américo Boavida
The Decree approves the Organic Statute of the Américo Boavida Hospital.
Regulation No 299/2013 Food, Medicine and Health Care Administration and Control
This regulation is issued to implement the Food Medicine and Health Care Administration and Control Proclamation No 661/2009. and covers among other aspects of food safety and quality which includes manufacturing, storage and transportation among other aspects; sale of alcohol; medicine administration and control which includes manufacturing, registration, storage, transportation, importation ad clinical trials among others; traditional and complementary medicine administration and control; post-marketing surveillance; control of tobacco products and places prohibited for smoking among other aspects.
Medicines and Related Products Act
The Act regulates the quality and safety of medicines and related products and connected matters.
The National Drug Policy and Authority (Issue of Licenses) Regulations
These Regulations govern the issuance of licenses for the importation, exportation, manufacture, distribution, and retail of drugs, etc.
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.
Décret No 0256/PR/MS du 19 juin 2012 portant attributions et organisation des centres hospitaliers régionaux
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.