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.

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.

These guidelines are for the general public and in particular, individuals intending to engage in the manufacture of packaged food products on a micro-scale. the document prescribes the minimum Good Hygiene Practices (GHP) requirements for the facilities, controls to be used in the manufacturing, processing and packaging of food products to ensure the safety of the product.

Vaccines and biologics should not be imported into Nigeria unless the facility has been inspected and found to comply with good storage practices and good distribution practices. Therefore, these guidelines prescribe the minimum requirements necessary for the inspection of a facility for compliance with GSP and GDP for the registration of vaccines, biologics and related products.

These guidelines are for the general public and in particular organizations intending to engage in the importation of cosmetics products under the global listing scheme. They cover small, medium, large and mega categories and also prescribe the minimum Good Hygiene Practice (GHP) and Good Storage Practice (GSP) requirements for the facilities used for storage and display of items cleared for global listing.