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.

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.

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 interest of the general public and in particular individuals and organizations intending to submit progress reports of ongoing clinical trials in Nigeria. The document emphasizes that progress reports on ongoing clinical trials in Nigeria should be submitted using the report template in This guideline.

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.

This document defines the terms “objective” and “study endpoint”. It clearly states that for purposes of registration and reporting, the terms objectives and endpoints as used in this template provided in this document align with the terms primary purpose and outcome measures in clinicaltrials.gov, respectively. Individuals should provide a description of the study objectives and endpoints, as well as a justification for selecting the particular endpoints, in the table format included in the statement of compliance 3.0 of the document. This will provide clear articulation on how the selected primary and secondary endpoint(s) are linked to achieving the primary and secondary objectives and an explanation of why endpoint(s) were chosen. Data points collected in the study should support an objective or have a regulatory purpose. Therefore, careful consideration should be given prospectively to the amount of data needed to support the study’s objectives.

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.