Filter by
- (-) Botswana (19)
- (-) Madagascar (7)
- (-) Namibia (12)
- Algeria (23)
- Angola (17)
- Benin (21)
- Burkina Faso (27)
- Burundi (15)
- Cabo Verde (20)
- Cameroon (22)
- Central African Republic (8)
- Chad (12)
- Comoros (8)
- Congo (18)
- Cote d'Ivoire (22)
- Democratic Republic of the Congo (22)
- Equatorial Guinea (9)
- Eritrea (6)
- Eswatini (11)
- Ethiopia (15)
- Gabon (33)
- Gambia (21)
- Ghana (24)
- Guinea (19)
- Guinea-Bissau (6)
- Kenya (48)
- Lesotho (17)
- Liberia (6)
- Malawi (14)
- Mali (23)
- Mauritania (18)
- Mauritius (22)
- Mozambique (35)
- Niger (42)
- Nigeria (16)
- Rwanda (58)
- Sao Tome and Principe (8)
- Senegal (28)
- Seychelles (15)
- Sierra Leone (11)
- South Africa (13)
- South Sudan (6)
- Togo (23)
- Uganda (18)
- United Republic of Tanzania (32)
- Zambia (8)
- Zimbabwe (11)
Medicines and related substances regulations
These Regulations provide rules on the registration and access to the market to medicine; licensing requirements for pharmaceutical operations, manufacturers, wholesalers and dispensaries; as well as on record-keeping, import of medicines, and clinical trials, etc.
Consumer Protection Act
The Act contains provisions to provide protection of the interests of consumers by means of investigation, prohibition and control of unfair business practices; and to provide for matters incidental thereto.
Data Protection Act
This Act regulates the protection of personal data and ensures that the privacy of individuals in relation to their personal data is maintained. It also establishes the Information and Data Protection Commission and provides for all matters incidental thereto.
Loi No 2018-027 relative à l’état civil
The purpose of this law is to provide for the rules relating to the civil status of citizens, civil status documents, as well as procedures for registering civil status events and their computerized management. It guarantees every person the enjoyment of the right to recognition in all places of their legal personality.
National Registration (Amendment) Act
This Act amends sections 2, 6, 7, 9, 12, 14, 17, 17A, 18 and 19 of the National Registration Act of 1986.
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.
National health quality standards for clinics - Management and leadership
The Botswana National Health Quality Standards for Clinics provide guidance on the topic of management and leadership in the governance of the health facility focusing on such areas as responsibilities and accountability of governing bodies; applicable laws and regulations; budgeting, reporting and auditing processes; planning of health services that correspond to the patient and population needs, etc.
National Health Quality Standards - Medical Care
The National Health Quality Standards for Hospitals provide guidelines for hospitals regarding coordination of patient care, facilities and equipment, clinical practice guidelines, assessment of patients, patient care, medication, etc.
Loi No 2014-038 sur la protection des données à caractère personnel
The purpose of this law is to protect the rights of individuals in the processing of personal data.
Public health Act
The Public Health Act repeals, re-enacts, consolidates and amends the law relating to public health in Botswana.
National Health Quality Standards - Standards and guidelines for emergency medical services
This document outlines the required standards and guidelines for delivering high-quality emergency medical services in Botswana, focusing on ensuring effective, timely, and consistent care across the healthcare system.
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.
National Health Quality Standards - Health care organizational management
The National Health Quality Standards - "Health Care Organizational Management" provide comprehensive guidelines for managing healthcare organizations in Botswana, covering areas such as governance, resource management, leadership, quality improvement, and compliance with regulatory standards to ensure effective and efficient delivery of healthcare services.
National Health Quality Standards - Diagnostic, Care and Treatment Support Services
The "National Health Quality Standards - Diagnostic, Care, and Treatment Support Services" establish guidelines and standards for the provision of diagnostic services, patient care, and treatment support in Botswana.
Essential drug list
These guidelines establish an Essential Drug List of Botswana of 2012 and provide the requirements regarding the levels of availability across health care providers.
Loi No 2011-002 portant Code de la Santé
The Law establishes the Health Code that codifies legislative texts concerning Public Health in Madagascar.
Loi No 2011-003 portant réforme hospitalière
The Law establishes provisions relating to the hospital reform and applies to all hospital establishments in Madagascar.
Constitution
The Constitution of Madagascar was adopted in 2010. It consists of 168 Articles that are grouped into seven titles. The Constitution addresses a wide range of issues such as the fundamental principles of the State, freedoms, rights and obligations of the citizens, organization of the State, key organs of the state, etc.
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.