Health Legislation

By this decree, the Government of Benin appoints the auditors of the National Health Insurance Agency.

This Proclamation is to provide for Food and Medicine Administration. It provides rules to regulate several areas including food, medicine, medical devices, cosmetics, and tobacco products.

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.

The law sets out the fundamental principles and rules for the organization and operation of the national public health system.

This order, which provides for the organization and governance of health structures in the Gabonese Republic, supplements order No 1/95 of January 14, 1995, providing guidance for health policy in the Gabonese Republic.

This Law establishes the Rwanda Food and Drugs Authority and determines its mission, organization and functioning. The authority has a legal personality and enjoys administrative and financial autonomy. 

This decree sets forth the principles and regulations for health units within the National Health Service. It outlines specific statutes for these units, differentiating between those operating as public business entities and those in the public administrative sector. The decree applies to all National Health Service entities in the healthcare network, including hospitals, hospital centers, local health units, and other establishments providing care to National Health Service users, under public-private partnership agreements.

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 establishes a unified health system, coordinates the inter-relationship between the national government and county government health systems, provides for regulation of health care service and health care service providers, health products and health technologies and for connected purposes.

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 law creates a public administrative establishment, called the "Agence Nationale de Sécurité Sanitaire", under the supervision of the Ministry of Health. The mission of the Agence is to implement the strategic orientations of the Ministry of Health in the field of health safety.

This decree establishes the Steering Committee for the implementation of the Universal Health Insurance Scheme and contains provisions concerning its composition as well as its departmental and regional structures.

This decree was adopted to implement the Law 2014-131 (universal health insurance) to establish the Social Security Institution ("institution de Prévoyance sociale").

The decree creates a multi-sectoral committee to combat counterfeiting and the illicit sale of medicines and other pharmaceutical products, reporting to Niger's Minister of Public Health.

The Health Professions Regulatory Bodies Act of 2013 establishes the Allied Health Professions Council, the Medical and Dental Council, the Nursing and Midwifery Council, the Pharmacy Council, the Psychology Council and provides for related purposes.

This Act makes provisions for the establishment of the Kenya Medical Supplies Authority and for connected purposes.

The decree establishes a Committee of Experts in charge of technical evaluation, whose mission is to carry out the technical evaluation of applications for registration of pharmaceutical products for human use. It also gives an opinion on the quality, safety and efficacy of pharmaceutical products for human use submitted for registration.

The decree creates the Commission Nationale du Médicament (CNM) for human use, whose mission is to validate the work of the Expert Committee responsible for the technical evaluation of applications for marketing authorization for pharmaceutical products for human use. It also gives a final opinion on marketing authorization applications; applications for renewal, extension of variation and transfer of marketing authorization; temporary suspension of marketing authorization; and proposals for definitive withdrawal of marketing authorization.

This Act establishes a Health Care Agency and provides for matters connected therewith or incidental thereto.