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 marketers of Pesticides, Agrochemicals, Fertilizers, Bio-pesticides and Bio-fertilizers in Nigeria.

The 2017 appropriation act highlighting the various Expenditures for the ministry of interior

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 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, 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, 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.

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 the application, verification of application, payment, submission and review of the application, endorsement, joint inspection of consignment, and release of the consignment.

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, companies that intend to dispose of unwholesome NAFDAC regulated products. It emphasizes that no regulated product 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.

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.

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

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 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.

The 2017 appropriation act highlighting the various Expenditures for the ministry of health

These guidelines are for the interest of the general public and manufacturers of veterinary cosmetics in Nigeria. It provides information on the application for inspection, procedures 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 and in particular manufacturers of veterinary medicinal cosmetics in Nigeria. The document outlines the 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, manufacturers of local animal feed, pet food and premixes. The document outlines the procedures for payment and application, inspection and labelling requirements.

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.