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Loi N°2021-12 du 20 Décembre 2021 modifiant et complétant la loi N° 2003-04 du 3 Mars 2003 relative à la santé sexuelle et à la reproduction
This Law provides amendments to the provisions of Articles 17, 17-1, 17-2, 17-3, 17-4, 17-5, 17-6, 17-7, 19-1 of the Law No 2003-04 of 03 March 2003 relating to sexual health and reproduction.
Loi No 2017-025 relative à la Santé de la Reproduction
This Law contributes to the protection of the present and future generations from the devastating health, social and health effects of diseases affecting public health and in particular reproductive health in the Islamic Republic of Mauritania. This Law is published in a collection of other legislative acts and can be found on page 4 of the file.
Lei No 12/2017 Lei de medicamento, vacinas e outros produtos biológicos para o uso humano
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.
Medicines and Related Products Act
The Act regulates the quality and safety of medicines and related products and connected matters.
Medicines and related substances Act
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.
Medicines and Related Substances Control Amendment Act
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.
Decreto-Lei No 59/2006
This decree regulates the marketing authorization, registration, manufacture, import, export, marketing, donations and advertising of medicines for human use.
Loi No 06.005 du 20 juin 2006 Bangayassi Relative à la Santé de la Reproduction
This law regulates reproductive health in the Central African Republic.
Loi No 2006-16 sur la Santé de la Reproduction au Niger
This law governs reproductive health in Niger. It sets out the principles of reproductive health, and regulates reproductive health structures, care and services, among other aspects.
Loi n° 049-2005/AN portant santé de la reproduction
The law governs reproductive health in Burkina Faso. It includes reproductive health care and services. It establishes rights and duties, as well as penal provisions.
Loi No 2005-18 du 05 aout 2005 relative à la santé de la reproduction
This Law contains provisions regulating reproductive health.
Loi No 2003-04 relative à la Sante Sexuelle et à la Reproduction
This Law provides provisions on the definition, principles and rights in reproductive health, defines reproductive health service entities and workforce, and regulates contraception, voluntary termination of pregnancy, rights of people suffering from STDs/AIDS and penal provisions.
Ley No 3/2003 de Medicamentos
The scope of application of this Law includes: medicines and health products, as well as the actions of natural and legal persons involved in the production, marketing, prescription and dispensing of pharmaceutical and health products within the national territory. This document is published as a part of a compilation of laws and decrees and this Law is located on page 2 of the file.
The Tanzania Food, Drugs and Cosmetics Act
This Act provides for the efficient and comprehensive regulation and control of food, drugs, medical devices, cosmetics, herbal drugs and poisons and repeals the Food (Control of Quality) Act, 1978, the Pharmaceuticals and Poisons Act, 1978, and provides for related matters.
Loi No 006/PR/2002 du 15 avril 2002 portant promotion de la santé de reproduction
The objective of this law is to define reproductive health and related entitlements.
Proclamation No 36/1993 to control drugs, medical supplies and sanitary items
This proclamation provides rules to control drugs, medical supplies and sanitary items.
The Medical Stores Department Act
This Act establishes the Medical Stores Department for the procurement, storage and distribution of medical supplies and provides for other matters connected or incidental to the establishment and management of the department.
Zimbabwe National Family planning Council Act
This Act establishes the Zimbabwe National Family Planning Council and provides for its structure, functions and powers. It further provides for reproductive health and family planning services in Zimbabwe and the promotion and implementation of population and development primary health care and other community-based development programmes relating to family health and for the integration and co-ordination of other relevant activities in Government departments, Nongovernmental organizations and the Private sector.
Medicines and Related Substances Act 101 of 1965
The Act provides for the registration and control of medicines and related substances for human and animal use, establishes the Medicines Control Council, and outlines its powers and responsibilities. It includes provisions for the licensing of manufacturers, distributors, and dispensers, as well as measures to ensure the availability of affordable medicines. The Act also addresses the regulation of medicine pricing, generic substitution, labeling, and procedures for appeals and re-evaluation of registered medicines.