The guideline has an overall objective to encourage and facilitate timely paediatric medicinal product development in Nigeria. It provides an outline of critical issues in paediatric drug development and the approaches to the safe, efficient and ethical study of medicinal products in the paediatric population.

This guideline document is for the interest of the general public and in particular, holders of the NAFDAC certificate of registration for regulated products, who may wish to grant authorization (No objection) for the importation of their registered products by another company.

These guidelines are intended to guide the technical and other general data requirements when applying for renewal of product licenses for imported medical devices. It outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market.

These guidelines are for the interest of the general public and in particular importers of donated products into Nigeria. The document provides information on the documentation for clearance, physical examination, and release of the consignment from the port of entry.

These guidelines are for the interest of the general public and in particular, importers of finished bulk food, food raw materials and animal feed into Nigeria. The document emphasizes that no finished bulk food and/or food raw materials should be imported without obtaining Import Permit. It also provides for payment, submission of documents for first endorsement, joint inspection of consignment, second endorsement, the release of consignment and tariff.

These guidelines are developed for the interest of the general public and in particular, importers of Narcotic and Controlled Substances, Pharmaceutical raw materials and restricted chemicals into Nigeria. The document emphasizes that pharmaceutical raw materials and restricted chemicals should not be imported without obtaining an Import permit and permit to clear where applicable.

These guidelines are for the interest of the general public and in particular, government agencies, international bodies & multinational companies who wish to import NAFDAC regulated products. It emphasizes that no food, drug, cosmetics, packaged water, detergent, the medical device shall be manufactured, imported, exported, advertised, sold, distributed or used in Nigeria unless it has been registered in accordance with the provisions of NAFDAC Act CAP N1 (LFN) 2004, other related Legislations and the accompanying guidelines.

These guidelines are for the interest of the general public and in particular importers of finished pharmaceutical, nutraceutical and herbal products (Human and Veterinary) into Nigeria. The document provides for payment, submission of documents for first endorsement, first endorsement, and joint inspection of consignment, second endorsement and release of the consignment.

This guideline document is for those importers of bulk food raw materials/importers of frozen fish, for which NAFDAC permits or certificates of registration are not issued, who require authorization to open from M.

These guidelines are for the interest of the general public and in particular, importers of food products into Nigeria. The document provides the procedures for application, verification of the application, payment, submission of application, review of the application, first endorsement, joint inspection of consignment, second endorsement, the release of consignment and tariff.

This document provides the implementation guidelines for containment of COVID-19 by the Federal Government of Nigeria at different phases of COVID-19 response measures. This is to curb the spread of coronavirus in work environments.

These guidelines are for the interest of the general public and in particular, importers of cosmetics and medical devices into Nigeria. The document emphasizes that no cosmetics and medical devices shall be manufactured, imported, exported, advertised, sold, distributed or used in Nigeria unless it has been registered under the provisions of the National Agency for Food and Drug Administration and Control (NAFDAC) Act CAP N1 (LFN) 2004, other related legislations and the accompanying guidelines.

These guidelines are for the interest of the general public and in particular to marketers of pesticides, agrochemicals, fertilizers, bio-pesticides and bio-fertilizers in Nigeria. It emphasizes that no importation shall be made by any importer of pesticides, agrochemicals, fertilizers bio-pesticides and bio-fertilizers without obtaining a listing certificate as a pesticide and agrochemical marketer from NAFDAC except under the provisions of NAFDAC Act CAP N1 (LFN) 2004, other related Legislations and the accompanying guidelines.

These guidelines are for the interest of the general public and in particular importers of general chemicals, agrochemicals and raw materials into Nigeria. The document emphasizes that no general chemicals, agrochemicals or raw materials shall be imported without obtaining an Import permit or approval. It provides for payment, submission of documents for first endorsement, joint inspection of consignment, second endorsement and release of the consignment.

These regulations apply to the labelling of food additives sold either by retail or others, including sales to caterers and food manufacturers. They also apply to food processing aids and also provide the prohibition regulation that no person can manufacture, import, export, distribute, advertise, display for sale or use any food additives, except food additives set out in the prescribed standards.

These regulations apply to all fortified foods manufactured, imported, exported, distributed, advertised, sold or used in Nigeria. The regulatory document provides for the advertisement of foods to which no vitamin and/or mineral has been added, label declaration of food to which vitamin and/or mineral has been added, a statement relating to the mineral content of food, label declaration of food mandatorily fortified with vitamin A, labelling, packaging, penalty and forfeiture after conviction.

These regulations apply to foods processed by ionizing radiation that is used in conjunction with applicable hygienic codes, food standards and transportation codes, manufactured, imported, exported, distributed, advertised, sold or used in Nigeria. The document provides information on the general requirement for food treatments, radiation sources, absorbed dose, facilities and control of the process, the wholesomeness of irradiated foods, packaging, quality assurance, inspection, re-irradiation, labelling, trade-in irradiated foods, importation, exportation, penalty, and forfeiture after conviction

These regulations apply to cocoa and cocoa products that are manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. The document provides information on labels, conditions for claims that food is cocoa-based, prohibitions, maximum limits of contaminants, permitted additives, penalty, and forfeiture after conviction.

These guidelines are for the interest of the general public and in particular, manufacturers of herbal remedies/dietary supplements made in Nigeria. The document emphasizes that no herbal remedies/dietary supplements shall be manufactured, imported, exported, advertised, sold, distributed or used in Nigeria unless it has been registered under the provisions of the National Agency for Food and Drug Administration and Control (NAFDAC) Act CAP N1 (LFN) 2004, other related Legislations and the accompanying guidelines.

These regulations apply to procedures and processes that will ensure appropriate importation, exportation, manufacturing, storage, warehousing, distribution, inspection, use for medical and scientific purposes, disposal as well as documentation of controlled medicines in Nigeria, in such a manner as to maintain the security and integrity of the product throughout the supply chain. They provide information on prohibition, application of registration, validity, Suspension or cancellation of certificate of registration, permit or authorization, importation of controlled medicines, labelling, storage facility, distribution, procurement, selection and quantification, inspection, dispensing disposal of controlled medicines, penalty, and forfeiture after conviction.