Policies / Policies from 2019
Policies with publication year 2019.
Ministry of Communications and Digital Economy
These regulations cover the processes and procedures for exercising monitoring and enforcement powers; consumer affairs and technical regulation; administrative fines; and procedures for revocation of license.
Ministry of Justice
This Act repeals the Prison Act Cap. P29 Laws of the Federation of Nigeria, 2004 and enacts the Nigerian Correctional Service Act to address new issues that are not covered under the repealed Act and provide clear rules setting out obligations of the Nigerian Correctional Service and the Rights of inmates.
Ministry of Finance, Budget and National Planning
This bill proposes major fiscal reforms to promote fiscal equity by mitigating instances of regressive taxation; reforming domestic tax laws; introducing tax incentives for investments in infrastructure and the capital market; supporting small businesses in line with the ongoing Ease of Doing Business reforms; raising revenues for the government by various fiscal measures including a proposed increase in the rate of Value Added Tax from 5% to 7.5%.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that herbal remedies/dietary supplements made in Nigeria products placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of herbal remedies/dietary supplements made in Nigeria outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. It is intended to provide guidance on the technical and other general data requirements when submitting an application for the renewal of a product license for herbal remedies/dietary supplements made in Nigeria.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that medical devices made in Nigeria placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of medical devices made in Nigeria outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. The guidelines are designed to provide guidance on the technical and other general data requirements when submitting an application.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that imported herbal remedies/dietary supplements placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of imported Herbal remedies/dietary supplements outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. It provides guidance on the technical and other general data requirements when submitting an application for the renewal of a product license for imported herbal products and dietary supplements.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that imported drugs placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of imported drugs outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. The document is designed to provide guidance on the technical and other general data requirements when submitting an application for renewal of product license for imported drugs.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that drugs made in Nigeria placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of drugs made in Nigeria outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. The document is intended to provide guidance on the technical and other general data requirements when submitting an application for renewal of product license for a drug made in Nigeria.
Ministry of Health
Provides a comprehensive framework for surveillance, case management, laboratory diagnosis, infection prevention, risk communication, and animal control to contain monkeypox outbreaks. Emphasizes coordination across human and animal health sectors using a One Health approach
Ministry of Health
Provides protocols for surveillance, lab testing, case management, vaccination, vector control, and outbreak response to prevent and contain yellow fever epidemics nationwide
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