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 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 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 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.

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.

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 Act establishes a national drug policy and a national drug authority to ensure the availability, at all times, of essential, efficacious and cost-effective drugs to the entire population of Uganda, as a means of providing satisfactory health care and safeguarding the appropriate use of drugs.

This Act is to establish a Medicines Control Authority of Zimbabwe and to confer functions on such Authority in relation to the registration of medicines; to provide for the Zimbabwe Regional Medicines Control Laboratory and for its functions; to provide for the appointment of a Director-General of the Authority and for the keeping of a Medicines Register; to provide for certain prohibitions, controls and restrictions relating to medicines and other substances; and to provide for matters connected with or incidental to the foregoing.