These guidelines have been designed for the general public and in particular, manufacturers of bread in Nigeria.

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 general public and in particular, companies involved in the processing and packaging of drinking water in Nigeria. The document prescribes the minimum Good Manufacturing Practice (GMP) requirements for the facilities and controls to be used in the processing of water to ensure that it is safe and meets quality standards.

These guidelines are for the interest of the general public and in particular, exporters of samples for machine trials. They provide information on application and issuance of export approval.

These guidelines are for the general public and in particular, manufacturers and packers of pre-packaged food in Nigeria. The document prescribes the minimum current Good Manufacturing Practice (cGMP) requirements for the facilities and controls to be used in the manufacture or processing of products to ensure that they meet quality standards.

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 timeline for obtaining permit.

These guidelines are for the interest of the general public and manufacturers of veterinary cosmetics in Nigeria. It provides information on application for inspection, procedure for payment, submission of application, scheduling of inspection and inspection.

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.

These guidelines are for the interest of the general public and in particular, manufacturers of local animal feed, pet food and premixes. The document outlines the procedures for payment and application, inspection and labelling requirements.

Fast track is an initiative of the Federal Government to facilitate trade and it is aimed at building local capacity in manufacturing and decongesting the ports. It is for the clearing of registered regulated products, bulk raw materials and packaging materials for registered regulated products. Therefore, this document provides information on application, verification of application, payment, submission and review of application, endorsement, joint inspection of consignment, and release of consignment.

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 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 practice and good distribution practice. 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 importation of cosmetics products under 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.

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 listing certificate as a pesticide and agrochemical marketer from 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 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 consignment.

These guidelines prescribe the minimum Good Manufacturing Practice (GMP) requirements for the facilities and controls to be used in the manufacture of products approved for this scheme to ensure quality and safety of the products. It states that regulated products should not be manufactured in Nigeria unless the facility has been inspected and a Certificate of Recognition as a manufacturer is issued by NAFDAC. The document highlights the only products to be manufactured and how to apply for inspection.

These guidelines are for the interest of the general public and in particular individuals and organizations intending to conduct clinical trials in Nigeria. This document emphasizes that no person shall import, procure or manufacture a drug product, cosmetic or medical device for the purpose of a clinical test in Nigeria unless he is a holder of a valid clinical trial approval and the trial is to be conducted in accordance with the terms of the approval and the provisions of any regulations in force.