Health Legislation

This Decree approves the amended statutes of the Beninese pharmaceutical regulatory agency, now named “Beninese Agency for Medicines and other Health Products”.

This Order provides for the creation, organization and operation of the program called the National Health Education Programme.

This Law amends Articles 1, 2, 3, 5, 6, 8, 9, 10, 11, 13, 14, 16, 18, 20, 21, 23, 25, 27, 31, 33, 36, 37, 38, 42, 45, 47, 51, 51, 52, 53, 54, 55, 56, 65, 66, 80 and 86 of the Law No 2020-37 protecting the health of people in the Republic of Benin.

The Decree sets out the statutes of the Nigerian Pharmaceutical Regulatory Agency.

This Decree establishes and fixes the rules of organization and operation of the Senegalese Pharmaceutical Regulatory Agency (ARP)

This Act repeals and replaces the Public Health Act of 1960, provides for the promotion, protection and improvement of public health and well-being in Sierra Leone, provides for the protection of individuals and communities from public health risks, provides for the prevention and control of the spread of infectious diseases, provides for local government and community participation in protecting public health, provides for early detection and prompt response to diseases and public health threats and provides for other related matters.

The purpose of this law is to organize the protection of the health of the population, and to define the obligations imposed on citizens in the event of communicable, non-communicable, contagious diseases or epidemics. It applies to any person living in the Republic of Benin or entering Benin territory.

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.

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.

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 Act lays down the fundamental provisions and principles and aims to give concrete form to the rights and duties of the population in matters of health. Its purpose is to ensure the prevention, protection, maintenance, restoration and promotion of people's health. It was published in the Official Journal on 29 July 2018.

This Law establishes the fundamental principles relating to the organization of public health in the Democratic Republic of the Congo.

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).

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.

The Public Health Act repeals, re-enacts, consolidates and amends the law relating to public health in Botswana.

The code provides rules regarding different rears of public health. It defines the rights and duties pertaining to the protection and promotion of the health of the population.

This Act provides for the promotion, preservation and maintenance of public health with a view to ensuring the provisions of comprehensive, functional and sustainable public health services to the general public; and provides for other related measures.

This Act provides for the establishment of a Namibia Medicines Regulatory Council; for the registration of medicines intended for human and for animal use; for the control of medicines and scheduled substances and provides for incidental matters.

This law provides the general framework for the action of the State in the area of health.