Policies / Policies from 2019
Policies with publication year 2019.
Ministry of Transportation
This document focuses on key issues that revolve around how emerging trends in the global maritime industry affects the shipping and maritime sector in Nigeria, domestic factors that will influence the sector and progress on the drive to mitigate challenges in the sector.
Ministry of Youth & Sports Development
The National Youth Policy recognises the broader policy context in which it has been formulated and shall operate. It is guided largely by other national policy initiatives and it is also reflective of international programmes and conventions. This policy is based on a commitment to extensive consultations, respect for diversity of interests and opinion, input and consensus from the grassroots and local communities in the spirit of national ownership. It affirms and upholds the fundamental human rights of all youth, including their rights to fundamental freedoms, development opportunities and full participation in the democratic and governance processes, as well as in community and civic decision-making and development agenda.
Ministry of Infrastructure
This scheme is a Public-Private Partnership intervention that enables the Federal Government of Nigeria to leverage private sector funding for the construction or refurbishment of eligible road infrastructure projects in Nigeria. It focuses on the development of eligible road infrastructure projects efficiently and effectively that creates value for money through private sector discipline and also guarantees participants in the scheme timely and full recovery of funds provided for the construction or refurbishment of eligible road infrastructure projects in the manner prescribed in this executive order.
Ministry of Industry, Trade and Investment
The purpose of this procedure is to describe the processes of management system certification (MSC) to meet the requirement of ISO 17021 - 1. This procedure applies to all management system certification services offered by the SON MSC. It covers SON MSC certification processes from initial application to continuing surveillance after certification has been achieved.
Ministry of Health, National Agency for food and Drug Administration and Control
These regulations apply to wine manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. It provides regulations on the use and limit of food additives, categories of grapevine, vintage dating, sugar content and labelling.
Ministry of Health, National Agency for food and Drug Administration and Control
These regulations apply to all spirit drinks, manufactured, imported, exported, distributed, advertised, sold or used in Nigeria. They also apply to the use of ethyl alcohol and distillates of agricultural origin in the production of alcoholic beverages and the use of the names of spirit drinks in the presentation and labelling of foodstuffs.
Ministry of Health, National Agency for food and Drug Administration and Control
These regulations apply to all foods containing fats and oils that are manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. It guides vitamin A fortification, source, additives, impurities and labelling of fats and oils
Ministry of Health, National Agency for food and Drug Administration and Control
Cold chain management is a specialized area of Biopharmaceutical products management that begins when a Biopharmaceutical product is manufactured, stored and moves through the distribution chain until it gets to the end-user at the time of administration. It is required that the product be held and distributed in a controlled environment. It is necessary to have adequate control of all steps and procedures involved both in manufacturing and quality control, storage and distribution, to ensure that product quality is maintained. Therefore, this document was designed to guide importers and owners of storage facilities for medicines that require cold chain management. This is to provide stakeholders with the relevant regulatory requirements needed to maintain the compliance status of their operational activities.
Ministry of Health, National Agency for Food and Drug Administration and Control
These guidelines are for the interest of the general public and in particular manufacturers/importers of drugs, vaccines and in-vitro diagnostics into the county which has been prequalified by the World Health Organization. This guideline is based on NAFDAC�s regulatory reliance policy on the adoption of a regulatory reliance mechanism to make regulatory decisions as it relates to the granting of marketing authorization. Clinical trial approval and conduct of Good Manufacturing Practice (GMP) Inspections.
Ministry of Health
Labelling is an important and integral part of the approval of a medicinal product. This also applies to the Investigational Medicinal Product (IMP) in Clinical Trials (CTs). The purpose of regulatory labelling requirements for investigational medicinal products (IMPs) in Clinical Trials (CTs) is to provide added value regarding the protection of the subjects, Identification of the IMP, traceability of the IMP, proper use of the IMP, identification of trial and proper documentation of the trial.
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