Health Legislation

This law defines the general regime for the prevention and control of smoking, establishing rules regarding the protection from exposure; the advertising; the prohibition of the promotion and sponsorship of recreational and cultural activities, and the labelling among other issues. 

This law relates to the fight against tobacco; it applies to tobacco growing, regulation of the manufacture, packaging, labelling, marketing and importing of tobacco and tobacco products, as well as advertising.

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 Act gives effect to the World Health Organization 's framework Convention on tobacco control.

This Law establishes modalities for controlling tobacco consumption and tobacco products that are manufactured in Rwanda as well as those imported so as to protect the Rwandan population’s life.

The law reinforces the fight against the use and consumption of tobacco and tobacco products in Burkina Faso. The scope of the law covers the industrial or supervised cultivation of tobacco, the manufacture, packaging, marketing and consumption of tobacco and tobacco products, and exposure to tobacco smoke.

This Act regulates the use, sale, manufacture, advertising and promotion of a tobacco product and provides for connected matters.

This Act controls the production, manufacture, sale, labelling, advertising, promotion and sponsorship of tobacco products, provides for the Tobacco Control Board, regulates smoking in specified areas and connected 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.

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

The purpose of this Act is to: a) protect the health of the population against the many debilitating and fatal diseases caused by tobacco; b) limit the population's access to tobacco and protect it from inducements to use tobacco and the smoking which may result; c) make the population aware of the dangers of tobacco use and exposure to tobacco smoke.

This Proclamation is to protect the present and future generations from the devastating health, social, environmental and economic consequences of tobacco consumption and exposure to tobacco smoke by providing a legal framework for tobacco control measures, and reduce significantly tobacco use and its consequent harm.

The scope of application of this Law includes: medicines and health products, as well as the actions of natural and legal persons involved in the production, marketing, prescription and dispensing of pharmaceutical and health products within the national territory. This document is published as a part of a compilation of laws and decrees and this Law is located on page 2 of the file.

This Act provides for the efficient and comprehensive regulation and control of food, drugs, medical devices, cosmetics, herbal drugs and poisons and repeals the Food (Control of Quality) Act, 1978, the Pharmaceuticals and Poisons Act, 1978, and provides for related matters.

This proclamation provides rules to control drugs, medical supplies and sanitary items.

This Act establishes the Medical Stores Department for the procurement, storage and distribution of medical supplies and provides for other matters connected or incidental to the establishment and management of the department.

The Act provides for the registration and control of medicines and related substances for human and animal use, establishes the Medicines Control Council, and outlines its powers and responsibilities. It includes provisions for the licensing of manufacturers, distributors, and dispensers, as well as measures to ensure the availability of affordable medicines. The Act also addresses the regulation of medicine pricing, generic substitution, labeling, and procedures for appeals and re-evaluation of registered medicines.