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.
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.
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.
These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.
The Pharmacy Council Act
This Act establishes the Pharmacy Council of Mauritius and provides for better regulation of the profession of pharmacists.
Public Health Act
This Act repeals and replaces the Public Health Act (Cap 198). The Act provides the legal framework for the protection and improvement of public health, regulates issues such as sanitation, disease control, environmental health and health care services.
These Regulations amend the Health Professionals Act of 2006 by repealing and substituting Schedule 1 of the Act dedicated to the enumeration of the categories of health professionals.
Health Care Agency Act
This Act establishes a Health Care Agency and provides for matters connected therewith or incidental thereto.
Public Health Authority Act
This Act establishes the Public Health Authority to regulate and monitor health-related services, and establishes the Public Health Authority Board and the Appeals Board, their functions, powers and procedures and provides for matters connected therewith or incidental thereto.
Clinical Trials Act
This Act regulates the conduct of clinical trials for medicinal products in Mauritius.
DNA Identification Act
This Act establishes the legal framework for the collection, analysis, and use of DNA samples for criminal investigations, paternity testing, and identification purposes and establishes the DNA Population Statistical Database, as well as the Unidentified and Missing Persons Database.
Tobacco Control Act
This Act regulates the use, sale, manufacture, advertising and promotion of a tobacco product and provides for connected matters.