Health Legislation

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.

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 Regulation sets up rules in the registration of drugs and related products manufactured, imported, exported, advertised, sold, distributed or used in Nigeria.  

Specifications for essential medicines supplies.

These Regulations provide rules on the registration and access to the market to medicine; licensing requirements for pharmaceutical operations, manufacturers, wholesalers and dispensaries; as well as on record-keeping, import of medicines, and clinical trials, etc.

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.

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.

These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.

This document provides guidelines on the supply of essential medicines in the Democratic Republic of Congo.

This Ministerial decree regulates the trade of pharmaceutical products in the Democratic Republic of the Congo.

This regulation is issued to implement the Food Medicine and Health Care Administration and Control Proclamation No 661/2009. and covers among other aspects of food safety and quality which includes manufacturing, storage and transportation among other aspects; sale of alcohol; medicine administration and control which includes manufacturing, registration, storage, transportation, importation ad clinical trials among others; traditional and complementary medicine administration and control; post-marketing surveillance; control of tobacco products and places prohibited for smoking among other aspects.  

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

These Regulations govern the issuance of licenses for the importation, exportation, manufacture, distribution, and retail of drugs, etc.

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

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 Diploma approves the Medicines Registration Manual. The purpose of the Manual is to (a) Standardize the procedures and activities relating to the registration of medicines; (b) Clarify the doubts that professionals have encountered when interpreting the Registration Regulations; (c) Support professionals in the field in carrying out their daily activities in a standardized way; (d) Support applicants in complying with registration and post-registration procedures; (e) to make the registration process an optimized and increasingly swift process. 

The Decree sets out the conditions for manufacturing and importing contraceptive products into Burkina Faso.