These guidelines are for the interest of the general public, and in particular manufacturers and importers of feed supplements, feed concentrates, feed additives, premixes and fish meal in Nigeria. The document emphasizes that no company is allowed to import bulk feed supplements, feed concentrates, feed additives, premixes and fish meal without due authorization.

These guidelines are for the interest of the general public and in particular, importers of precursor chemicals into Nigeria. The document outlines the process for obtaining a permit to import precursor chemicals under the various international conventions and treaties and those controlled nationally.

These guidelines are for the interest of the general public, and in particular manufacturers and importers of feed supplements, feed concentrates, feed additives, premixes and fish meal in Nigeria.

These guidelines are for the interest of the general public and in particular, importers of narcotic drugs, controlled/psychotropic substances and drug precursors into Nigeria. The document emphasizes that narcotics, controlled/psychotropic substances and/or drug precursors should not be imported without obtaining an import permit and permit to clear where applicable.

This guideline document is designed for the interest of the general public and in particular companies that want to conduct field trial on products for registration purpose. It should be emphasized that no fertilizers, bio-fertilizers, pesticides, bio-pesticides or premixes shall be manufactured for commercial purpose, imported, exported, distributed, sold or used in Nigeria except it has been subjected to field trials at approved institute and monitored by the agency in accordance with the provisions of 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, importers of precursor chemicals into Nigeria. The document outlines the process for obtaining a permit to import precursor chemicals under the various international conventions and treaties and those controlled nationally.

These guidelines are for the general public and in particular persons intending to obtain permit to import industrial and laboratory chemicals. They prescribe the requirements for documentation, processing, personnel and timeline for obtaining permit to import laboratory and industrial chemicals.

These guidelines are for the interest of the general public and in particular, importers of narcotic and controlled substances into Nigeria. The document emphasizes that narcotics and controlled substances should not be imported without obtaining import permit and permit to clear where applicable and the steps in this guideline should be followed when the Federal Ministry of Health (FMOH) awards a contract to any organization/company to import on its behalf.

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 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.

The purpose of this guideline is to strengthen NAFDAC system for effective post marketing surveillance of medicines, and regulated products including medical devices to ensure that only quality and safe medicines and other regulated products are distributed throughout the country. The implementation of This guideline will enable NAFDAC generate scientific evidence on the quality and safety of medicines and medical devices for improved health outcome.

This document is designed to provide labelling procedures for packed medicinal products

These guidelines are for the interest of the general public and in particular the Pharmaceutical Manufacturing companies in Nigeria. They prescribe the minimum requirements necessary for the issuance of authority to manufacture pharmaceutical products.

These guidelines are for the interest of the general public and in particular marketers of Pesticides, Agrochemicals, Fertilizers, Bio-pesticides and Bio-fertilizers in Nigeria.

These guidelines are for the interest of the general public and in particular the pharmaceutical manufacturing companies in Nigeria. The document prescribes the minimum requirements necessary for the inspection of a facility for compliance with good manufacturing practices for the registration of pharmaceutical products.

These guidelines are for the interest of the general public and in particular, animal feed toll millers in Nigeria. The document emphasizes that no unbranded animal feeds shall be produced in Nigeria unless the production facility and process have been inspected and the facility listed by NAFDAC except 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 to animal feed toll millers in Nigeria. It emphasizes that no unbranded animal feeds shall be produced in Nigeria unless the production facility and process have been inspected and the facility listed by NAFDAC 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 manufacturers of medicated feed in Nigeria. The document provides information on procedures for application, submission, scheduling of inspection, tariffs and labelling.

These guidelines are for the interest of the general public, NAFDAC clients or stakeholders who wish to make a complaint or make an appeal in the case of a regulatory decision regarding products and/or issues relating to NAFDAC regulated products.

These guidelines are for the interest of the general public and in particular manufacturers of veterinary medicinal cosmetics in Nigeria. The document outlines procedure for payment, submission of applications, scheduling of inspection, inspection and labelling.

These guidelines are for the interest of the general public and in particular, for travelers wishing to obtain export approval for NAFDAC regulated products including food stuff not pre-packaged (e.g. crayfish, pepper, etc.) for personal use. It emphasizes that NAFDAC will not issue any export approval for products that have already left the shores of the country.