This Decree approves the amended statutes of the Beninese pharmaceutical regulatory agency, now named “Beninese Agency for Medicines and other Health Products”.
The Act amended the National Identity Cards Act, 2011.
The Decree sets out the statutes of the Nigerian Pharmaceutical Regulatory Agency.
The document establishes the Paediatrics treatment guidelines in Rwanda.
This Decree establishes and fixes the rules of organization and operation of the Senegalese Pharmaceutical Regulatory Agency (ARP)
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.
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.
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.
The Guidelines provide requirements to provide private emergency medical services or private ambulance services in Rwanda.
The purpose of the Act is to establish a biometric identification and authentication system for natural persons.
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.
This Law amended the Law n°14/2008 governing registration of the population and issuance of the national identity card.
The law institutes in Burkina Faso an Economic Community of West African States (ECOWAS) biometric identity card with an electronic chip. The ECOWAS identity card is an official identification document required for all civil acts.
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).
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.
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.
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.
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.
This Law establishes a biometric identity card.
The Botswana National Health Quality Standards for Clinics provide guidance on the topic of management and leadership in the governance of the health facility focusing on such areas as responsibilities and accountability of governing bodies; applicable laws and regulations; budgeting, reporting and auditing processes; planning of health services that correspond to the patient and population needs, etc.