Health Legislation

This Decree establishes a general population registry in the Democratic Republic of the Congo.

This Decree contains provisions for the organization and operation of a public establishment called the Health Solidarity Fund in the Democratic Republic of the Congo.

This Decree regulates the organization and operation of the Regulatory and Control Authority for Universal Health Coverage of the Democratic Republic of the Congo. This document is published as a part of the Official Journal and the Decree is located on page 12 of the file.

This Decree regulates the organization and operation of a public institution called the Health Promotion Fund. This document is published as a part of the Official Journal and the Decree is located on page 23 of the file.

This Decree regulates the organization and operation of a public establishment called the National Institute of Public Health. This document is published as a part of the Official Journal and the Decree is located on page 31 of the file.

This Ordinance regulates the establishment, organization and functioning of the National Council for Universal Health Coverage in the Democratic Republic of the Congo.

This Law establishes the fundamental principles relating to the organization of public health in the Democratic Republic of the Congo.

This document provides guidelines on pharmacovigilance in the Democratic Republic of Congo.

The South Sudan Essential Medicines List (SSEML) is a comprehensive list of medications essential for addressing the country's public health needs, prioritizing safe, effective, and affordable treatments for the most common health conditions.

The Namibia Essential Medicines List acts as a guide for the level of availability and use of essential medicines based on the skills levels of health workers as well as the availability of diagnostic facilities at the various levels of the Namibian public sector healthcare system.

This Ministerial Decree regulates information and advertising of medicines and other health 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 Act provides a framework for a structured uniform health system within Namibia; consolidates the laws relating to state hospitals and state health services, and regulates the conduct of state hospitals and state health services; provides for financial assistance for special medical treatment of State patients; and provides for incidental matters.

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.

These Regulations outline the rules for acquiring nationality, issuance of the nationality certificates, loss of nationality, civil registry of the South Sudanese nationals, etc.

The Constitution of South Sudan was adopted in 2011. It is the supreme law of the state. The Constitution sets out the values and principles of organization of the state, establishes the rights, freedoms and obligations of the people, sets up key state institutions and bodies, etc. The Constitution of South Sudan consists of 200 articles that are grouped into fifteen parts, supplemented by 5 schedules.

The purpose of this Act is to determine the fundamental principles relating to the protection of the rights of people living with HIV/AIDS and of persons affected.

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.