These guidelines are for the interest of individuals intending to engage in the manufacturing of cosmetics and related products in Nigeria. the document prescribes the minimum Good Manufacturing Practice (GMP) requirements for the facilities and controls to be used in the manufacture of these products to ensure quality and safety. It also prescribes the requirements for conducting a production inspection of the cosmetics manufacturing facility.

These guidelines are for the interest of the general public and in particular, manufacturers of animal feed made in Nigeria. They emphasize that no animal feed shall be manufactured, imported, exported, advertised, sold, distributed or used in Nigeria unless it has been registered 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, pharmaceutical industries in Nigeria. The document provides guidelines for the registration of biosimilars in Nigeria.

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.

These guidelines are for the interest of the general public and in particular, manufacturers of medical devices made in Nigeria.

These guidelines are for the general public and in particular persons intending to renew permits to import industrial and laboratory chemicals. These guidelines prescribe the requirement for documentation, processing, personnel requirement, and timeline for obtaining a permit.

These guidelines are for the interest of the general public and in particular, industries in Nigeria that have registered regulated products. The document outlines the guidelines for the advertisement of NAFDAC regulated products

These guidelines are for the interest of the general public and in particular manufacturers of veterinary drugs in Nigeria. The document outlines the application for inspection, the procedure for payment, scheduling of inspection, inspection and labelling information.

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 importers of animal feeds, feed additives, feed concentrates, feed supplements, premixes, fish meal, pesticides, agrochemicals and fertilizers. The document outlines the application process, procedures of warehouse inspection etc.

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.

These guidelines are for the interest of the general public and in particular exporters of drugs, food, cosmetics, medical devices and other regulated products intended for commercial purposes. The document emphasizes that National Agency for Food and Drug Administration and Control (NAFDAC) will not issue any Export Approval for products that have already left the shores of the country. It also outlines the procedures for application, inspection and issuance.

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, 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.

The purpose of this guideline is to strengthen the 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 to generate scientific evidence on the quality and safety of medicines and medical devices for improved health outcomes.

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.

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.