These guidelines are for the interest of the general public and in particular, importers of Pesticides in Nigeria. It emphasizes that no pesticide product shall be manufactured, imported, advertised, sold, distributed or used in Nigeria unless it has been registered in accordance with the provisions of NAFDAC. The document outlines guidelines for the registration of imported pesticides, import permits and labelling

These guidelines are for the interest of the general public in particular and manufacturers of pesticides made in Nigeria. The document emphasizes that no Pesticide product shall be manufactured, imported, advertised, offered for sale, distributed or used in Nigeria unless it has been registered in accordance with the provisions of NAFDAC Act CAP N1 (LFN) 2004, other related legislations and the accompanying guidelines.

The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that drugs made in Nigeria placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of drugs made in Nigeria outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. The document is intended to provide guidance on the technical and other general data requirements when submitting an application for renewal of product license for a drug made in Nigeria.

The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that imported drugs placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of imported drugs outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. The document is designed to provide guidance on the technical and other general data requirements when submitting an application for renewal of product license for imported drugs.

The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that imported herbal remedies/dietary supplements placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of imported Herbal remedies/dietary supplements outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. It provides guidance on the technical and other general data requirements when submitting an application for the renewal of a product license for imported herbal products and dietary supplements.

The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that medical devices made in Nigeria placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of medical devices made in Nigeria outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. The guidelines are designed to provide guidance on the technical and other general data requirements when submitting an application.

The National Agency for Food and Drug Administration and Control has the responsibility of ensuring that herbal remedies/dietary supplements made in Nigeria products placed on the Nigerian market for use meet the requirements for quality, safety and efficacy throughout the lifecycle of the product. The procedure for registration of herbal remedies/dietary supplements made in Nigeria outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market. It is intended to provide guidance on the technical and other general data requirements when submitting an application for the renewal of a product license for herbal remedies/dietary supplements made in Nigeria.

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

These guidelines are for the interest of the general public and in particular the pharmaceutical manufacturing companies in Nigeria. The document prescribes the minimum requirements necessary for the inspection of a facility for compliance with good manufacturing practices for the registration of pharmaceutical products.

These guidelines are for the interest of individuals intending to engage in the manufacturing of herbal medicines and related products in Nigeria. This guidance document prescribes the minimum Good Manufacturing Practice (GMP) requirements for the facilities and controls to be used in the manufacture of herbal medicines and related products to ensure quality and safety. It also prescribes the minimum requirements necessary for inspection of a facility for compliance with good manufacturing practices for the registration of herbal medicine and related products.

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.

The 2017 appropriation act highlighting the various Expenditures for the ministry of labour and employment

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.