The purpose of this ordinance is to determine the rates and fees for regulatory services offered on drugs and other health products by the drug regulatory authority for Burundi (ABREMA).
The purpose of this ordinance is to organize the registration of medicines for human use and other pharmaceutical inputs in Burundi.
This Decree sets the operation modalities for some health competencies transferred by the State to the regions.
This document provides the list of essential medicines.
The purpose of this law is to regulate immigration and emigration in Burundi.
The law creates the Burundian Authority for the Regulation of Medicines for Human Use and Food. The authority's general aim is to protect public health by promoting the quality and safety of products such as prefabricated and ambient foods, medicines for human use, cosmetics and dietary products containing active ingredients, herbal medicines, traditional medicines, and medical devices, among others.
The decree provides for the organization and functioning of the Central Purchasing Center for Essential Medicines of Burundi [CAMEBU].
The decree regulates the establishment, organization and functioning of the National Public Health Institute of Burundi.
The law institutes a Social Protection Code in Burundi.
The legislation regulates the production, import, export, conservation, distribution, quality analysis and sale of medicines for human use, including traditional medicines, as well as all other health products, pharmaceutical practice and opticianry.
The Decree defines the normative framework for the organization and operation of the Ministry of Public Health and the fight against AIDS.
This Order provides for the creation of the Centre de Coordination des Opérations d'Urgences de Santé abbreviated to ‘CCOUSP’ (coordination center for health emergency operations).
Loi No 1/012 du 30 mai 2018 portant Code de l'offre des soins et services de sante au Burundi
The law sets out the fundamental principles and rules for the organization and operation of the national public health system.
Loi No 1/03 du 10 janvier 2018 portant promotion et protection des droits handicapées au Burundi
The aim of the law is to promote and protect the rights of persons with disabilities for their effective integration, so that their dignity is preserved and they can benefit from conditions that enable them, where appropriate, to be useful to themselves, their families, their communities and society as a whole by breaking down barriers of all kinds.
Namibia Essential Medicines List
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.
National Health Act
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 decision by the minister of public health provides for pricing scheme for the treatment of severe malaria.
This decree governs the organisation of the Ministry of Public Health and addresses among other things, the missions of the ministry (art. 1) and its structure (general structure is fleshed out under article 2).
This decision by the minister of public health provides the prices and conditions of availability of rapid malaria diagnosis kits.
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.