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Health Legislation

Health Legislation

Results (30)

The Resolution approves the Health Policy and the Strategy for its Implementation.

The Decree adopts the National Strategy for University Health Coverage in Niger 2021-2030.

The Regulation sets up rules in the registration of drugs and related products manufactured, imported, exported, advertised, sold, distributed or used in Nigeria.  

Specifications for essential medicines supplies.

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.

The objective of the law is to provide the general orientation, the principles and fundamental objectives of the State for Health. It considers the international commitments to which the country adhered to.

This Guide provides a comprehensive framework to enhance strategic planning, resource allocation, and performance evaluation, ensuring effective implementation of health programs and improved health outcomes.

The decree approves the National Financing Strategy for Universal Health Coverage and its 2018-2022 Action Plan.

The decree approves the national strategy for financing universal health coverage and its action plan 2018-2022.

Lei No 09/2018 Lei Base de Saude

This Law establishes the fundamental principles, rights, and responsibilities for the country's healthcare system, and provides for the overall organization of health care in the country. It also establishes provisions relating to the formulation of the national health policy as well as provides for the creation of the National Health Council.

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.

These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.

This document provides guidelines on the supply of essential medicines in the Democratic Republic of Congo.

This Ministerial decree regulates the trade of pharmaceutical products in the Democratic Republic of the Congo.

This regulation is issued to implement the Food Medicine and Health Care Administration and Control Proclamation No 661/2009. and covers among other aspects of food safety and quality which includes manufacturing, storage and transportation among other aspects; sale of alcohol; medicine administration and control which includes manufacturing, registration, storage, transportation, importation ad clinical trials among others; traditional and complementary medicine administration and control; post-marketing surveillance; control of tobacco products and places prohibited for smoking among other aspects.  

Medicines and Related Products Act

The Act regulates the quality and safety of medicines and related products and connected matters.

These Regulations govern the issuance of licenses for the importation, exportation, manufacture, distribution, and retail of drugs, etc.

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.

The Decree adopts the National Health Policy 2010-2025. The general objective of the National Health Policy (NHP) is to establish, define and outline guidelines for improving the population's state of health and quality of life in order to achieve the vision of a healthy life for all.

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. 

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