Health Legislation

The purpose of this law is to organize activities related to medicines and other health products in the Republic of Benin.

The Insurance Act of 2021 establishes the National Insurance Commission, and provides for the regulation and supervision of the insurance market and related matters.

The Law makes the first amendment to the Law no. 41/VI/2004, of April 5, which establishes the foundations of the National Health Service.

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 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.

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 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 Act regulates the quality and safety of medicines and related products and connected matters.

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.

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.

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

This Act establishes the Public Health Authority to regulate and monitor health-related services, and establishes the Public Health Authority Board and the Appeals Board, their functions, powers and procedures and provides for matters connected therewith or incidental thereto.

This Act provides for the establishment of an independent Drug and Food Control Authority in South Sudan and provide an appropriate and effective independent regulatory mechanism to control and regulate the manufacture, supply, promotion, marketing, advertising, distribution and use of drugs, poisons, chemicals, cosmetics medical devices and food for human or animal use.

The Health Institutions and Facilities Act of 2011 provides for a Health Facilities Regulatory Agency to license facilities for the provision of public and private health care services, establishes the Mortuaries and Funeral Facilities Agency to control and regulate facilities connected with the storage and disposal of human remains, establishes an Ambulance Council to regulate the operation of ambulance services in the country in accordance with policy standards and to provide for related matters.

The National Accreditation Board Act of 2007 establishes the National Accreditation Board and provides for related purposes.

This Act amends the Medicines and Related Substances Control Act, 2003, so as to amend and delete certain definitions; provides for a period within which the Council must be appointed; provides for the appointment of chairpersons of committees established by the Council; amends provisions relating to the classification of medicines and other substances as scheduled substances; amends provisions relating to the manufacturing, packing and selling of specified Schedule 3 and specified Schedule 4 substances; deletes references to generic substitutions; substitutes references to Schedule 1, Schedule 2, Schedule 3 or Schedule 4 medicines by references to Schedule 1, Schedule 2, Schedule 3 or Schedule 4 substances; inserts provisions relating to the registration of premises engaged in the manufacturing of medicines; amends provisions relating to offences and penalties; amends provisions relating to the destruction of forfeited medicines, scheduled substances or other things; provides for the making of regulations in relation to medicines; amends provisions relating to the exclusion of medicines from the operation of the Act; amends the transitional provisions; amends provisions relating to the repeal and amendment of certain laws; and provides for matters incidental thereto.

The Act provides for the establishment of the Council to regulate the conduct of Optometrists and Ophthalmic Opticians, the registration of Optometrists and Ophthalmic Opticians and provides for related matters.

This decree regulates the marketing authorization, registration, manufacture, import, export, marketing, donations and advertising of medicines for human use.