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Loi No 2010-022 du 10 février 2010 relative a la pharmacie
This Law defines the legal provisions relating to medicines, medical devices, other health products and the practice of pharmacy in the Islamic Republic of Mauritania. This Law is published in a collection of other legislative acts and can be found on page 3 of the file.
Diploma Ministerial No 223/2010 Aprova o Manual de Registo de Medicamentos
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.
Règlement No 06/2010/CM/UEMOA relatif aux procédures d’homologation des produits pharmaceutiques à usage humain
The purpose of the Regulation is to define the procedures for approving pharmaceutical products for human use in the member states of the West African Economic and Monetary Union.
Minimum Standards for Courses of Study for the Bachelor of Nursing Science Program
This document sets out the minimum standards for courses and the curricula for the Bachelor of Nursing Science Program in Uganda.
The Nursing and Midwifery Act
This Act makes provisions for the protection, promotion and preservation of public health, safety and welfare through regulation and control of nursing and midwifery education and practice.
Décret n° 2009-720/PRES/PM/MS/MEF/MCPEA portant conditions de fabrication et d'importation des produits contraceptifs au Burkina Faso
The Decree sets out the conditions for manufacturing and importing contraceptive products into Burkina Faso.
Liste Nationale des médicaments essentiels en République Centrafricaine
This document establishes a National List of Essential Medicines in the Central African Republic.
Food, Medicine and Health Care Administration and Control Proclamation No. 661/2009
This Proclamation regulates activities in respect of food, medicine, environmental health, health professionals, health and controllable health related institutions in the country.
Décret 2008/062/ PRG/SGG portant statut particulier du personnel de la santé
The Decree governs, among other aspects, the functions, competencies, working conditions, and remuneration of professionals in charge of promotion, prevention, and care activities in the public sector.
Law No 25/2008 establishing the National Council of Nurses and Midwives and determining its organisation, functioning and competence
This Law establishes the National Council of Nurses and Midwives and determines its organisation, functioning and competence.
The Medical Practitioners and Dental Surgeons (Amendment) Act
This Act amends the Medical Practitioners and Dental Surgeons Act, 1994.
National Accreditation Board Act, 2007 Act 744
The National Accreditation Board Act of 2007 establishes the National Accreditation Board and provides for related purposes.
Nutritionists and Dieticians Act
This Act provides for the training, registration and licensing of nutritionists and dieticians; provides for the regulation of the standards, and practice of the profession; ensures their effective participation in matters relating to nutrition and dietetics, and for connected purposes.
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.
The Pharmacy and Drugs (Amendment) Act
This Act amends section 38 of the Pharmacy and Drugs Act of 2001.
The Environmental Health Practitioners (Registration) Act
This Act provides for the establishment of the Council to regulate the conduct of and the registration of Environmental Health Practitioners and provides for related matters.
The Optometry Act
The Act provides for the establishment of the Council to regulate the conduct of Optometrists and Ophthalmic Opticians, the registration of Optometrists and Ophthalmic Opticians and provides for related matters.
Arrêté No 67 fixant les conditions d'exercice personnel de la profession de pharmacien d'officine
The order N°67 sets the conditions of practice of the profession of retail pharmacist. The text of the order is provided as part of a compendium of pharmaceutical legislation (see pages 6 and 7).
Circulaire No 12 MSPRH/MIN relative à l'exercice de la profession de pharmacien d'officine
The circular N°12 refers to inspections conducted in retail pharmacies. The text of the circular is provided as part of a compendium of pharmaceutical legislation (see pages 7 to 9).
Decreto-Lei No 59/2006
This decree regulates the marketing authorization, registration, manufacture, import, export, marketing, donations and advertising of medicines for human use.