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 an 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.

These guidelines are for the general public and in particular, for manufacturers of pre-packaged food products on a small scale in Nigeria. It prescribes the minimum Good Hygiene Practices (GHP) and Good Manufacturing Practice (GMP) requirements for the facilities, controls to be used in manufacturing, processing and packaging of food products to ensure the safety of the product.

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.

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

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, holders of NAFDAC certificates of registration for regulated products, who wish to grant authorization (no objection) for the importation of their registered products by another company. These guidelines are also for those importers of NAFDAC regulated products, for which NAFDAC Permits or certificates of registration are not issued, who require authorization to open form M and pre-arrival assessment report (PAAR).

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, exporters of samples for machine trials. They provide information on the application and issuance of export approval.

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 under the provisions of NAFDAC Act CAP N1 (LFN) 2004, other related Legislations and the accompanying guidelines.

These guidelines are for the general public and in particular persons intending to obtain a permit to clear restricted chemicals and agrochemicals. They prescribe the requirement for documentation, processing, personnel requirement, and the timeline for obtaining a permit.

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 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 manufacturers and importers of pesticides, agrochemicals and fertilizers in Nigeria. The document emphasizes that no company can import bulk pesticide, agrochemical or fertilizer without due authorization. Therefore, it provides guidelines involved in the application, processing and issuance of permits.

These guidelines are for the interest of the general public and in particular, persons or organisations in Nigeria intending to be listed as a Chemical manufacturer. The document aims to explain in simple terms the obligations on documentation, personnel requirement, safety standard and provides useful specifications with requirements on how to be listed as a manufacturer.

These guidelines are for the interest of the general public, and in particular manufacturers and importers of pesticides, agrochemicals and fertilizers in Nigeria. The document emphasizes that no company can import bulk pesticide, agrochemical or fertilizer without due authorization.

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 a permit to clear where applicable.

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 a fish meal without due authorization.

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.

This guideline document is designed for the interest of the general public and in particular companies that want to conduct field trials on products for registration purposes. 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 an approved institute and monitored by the agency under 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 general public and in particular persons intending to obtain a permit to import industrial and laboratory chemicals. They prescribe the requirements for documentation, processing, personnel and timeline for obtaining a permit to import laboratory and industrial chemicals.

Investigational medicinal products, which are unregistered medicines, can only be brought into the country after a positive ethical opinion is obtained, the clinical trial application has been approved and a letter of authorization has been issued by NAFDAC. Therefore, this guideline applies to all investigational medicinal products, including vaccines, which do not have marketing authorization in the country of intended use. It provides information on the responsibilities of the sponsor, labelling and packaging, importation and documentation procedures.