Health Legislation

This document provides the national list of essential medicines and other health products in Ethiopia. 

Specifications for essential diagnostic supplies.

Specifications for essential medicines supplies.

The Data Protection (Civil Registration) Regulations were developed in exercise of powers conferred by section 71 of the Data Protection Act, 2019 by the Cabinet Secretary for Information, Communication, Technology, Innovation and Youth Affairs.

These rules are issued in the exercise of powers conferred by section 16 of the Registration of Persons Act by the Cabinet Secretary for Interior and Coordination of National Government.

The Decree approves the Organic Statute of the Autoridade Nacional Reguladora de Medicamento (The National Medicines Regulatory Authority). The purpose of this Decree is to define the rules governing the organization, management and operation, as well as the powers of its bodies.

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.

The decree creates a National Technical Committee responsible for the administration of the District Health Information System in Niger. Its mission is to ensure the administration and updating of the platform; to identify and deal with users' technical grievances and concerns, and to ensure the system's security, maintenance and capacity building.

The document establishes the national list of essential medicines in Nigeria.

This document establishes the national list of essential medicines for children in Nigeria.

This Law is an amendment to Law No 32/2016 of 28/08/2016 governing persons and family.

This document provides a second edition of the List of Essential Medicines in Sao Tome and Principe.

The purpose of the Act is to establish a biometric identification and authentication system for natural persons.

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.

This law, published in the Official journal on 7 November 2019, is to put in place a system to ensure the protection of the fundamental rights and freedoms of individuals, in particular their privacy, with regard to the processing of personal data; and to ensure that information and communication technologies remain at the service of the citizen and do not infringe individual freedoms.

This Proclamation is to provide for Food and Medicine Administration. It provides rules to regulate several areas including food, medicine, medical devices, cosmetics, and tobacco products.

The Right to Information Act of 2019 provides for the implementation of the constitutional right to information held by a public institution, subject to the exemptions that are necessary and consistent with the protection of the public interest in a democratic society, to foster a culture of transparency and accountability in public affairs and to provide for related matters.

This decree establishes interoperability mechanisms for synergy of action between civil registry services and health structures across all the regions of the country.

This Act gives effect to Article 31(c) and (d) of the Constitution; establishes the Office of the Data Protection Commissioner; makes provision for the regulation of the processing of personal data; provides for the rights of data subjects and obligations of data controllers and processors; and for connected purposes.

This Act establishes the Pharmacy and Medicines Regulatory Authority; provides for the functions and powers of the Authority; and provides for matters connected therewith and incidental thereto.