These regulations apply to cocoa and cocoa products that are manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. The document provides information on labels, conditions for claims that food is cocoa-based, prohibitions, maximum limits of contaminants, permitted additives, penalty, and forfeiture after conviction.

These regulations apply to procedures and processes that will ensure appropriate importation, exportation, manufacturing, storage, warehousing, distribution, inspection, use for medical and scientific purposes, disposal as well as documentation of controlled medicines in Nigeria, in such a manner as to maintain the security and integrity of the product throughout the supply chain. They provide information on prohibition, application of registration, validity, Suspension or cancellation of certificate of registration, permit or authorization, importation of controlled medicines, labelling, storage facility, distribution, procurement, selection and quantification, inspection, dispensing disposal of controlled medicines, penalty, and forfeiture after conviction.

These regulations apply to all advertisements and promotion of cosmetics products (both single and compound entity) manufactured, imported, exported, sold, distributed or used in Nigeria.

These regulations provide for the registration of all cosmetics manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. It provides information on labelling information and the net content of cosmetic products.

These regulations guide the manufacture, import, export and distribution of safe cosmetics products and penalties for offenders of the regulations.

This document provides the Nigerian Nuclear Regulatory Authority (NNRA) minimum requirements for authorization of diagnostic radiology facilities in Nigeria. It states that the requirements should be applied in addition to the Nigerian Basic Ionizing Radiation Regulations 2003; the Nigerian Radiation Safety in Diagnostic and Interventional Radiology Regulations 2006; the Nigerian Radiation Safety in Radiotherapy Regulations 2006; and the Nigerian Radiation Safety in Nuclear Medicine Regulations 2006.

This document provides the Nigerian Nuclear Regulatory Authority (NNRA) requirements for authorization of diagnostic radiology practice.

Nigerian Nuclear Regulatory Authority (NNRA) requirement for registration of drilling rig to an NNRA authorized client. It emphasizes that NNRA requires that rig owners intending to lease their rigs for storage or handling of radioactive sources to only one NNRA licensed client with valid authorization need to obtain a certificate of registration of premises for those rigs.

The 2017 appropriation act highlighting the various Expenditures for the FCSC

These regulations apply to all advertisements or promotion of drug products both single and compound entities, manufactured, imported, exported, sold, distributed or used in Nigeria. It emphasizes that no person shall advertise any drug or related product unless it has been registered by the Agency. No person shall advertise any drug product unless the advertisement has the pre-clearance and approval of the Agency; and no person shall engage in consumer promotions of any kind, including but not limited to gifts or free samples of drug or related products to the consuming public.

These regulations apply to all labelling of drugs and related products manufactured, imported, exported, sold, distributed or used in Nigeria. No person can manufacture, import, export, distribute, advertise, display for sale or use any drug or drug product unless it is labelled per these regulations.

These regulations apply to the registration of drugs and related products manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. The document emphasizes that no drug product shall be manufactured, imported, exported, advertised, sold, distributed or used in Nigeria unless it has been registered under the provisions of these regulations.

These regulations apply to the labelling of food additives sold either by retail or others, including sales to caterers and food manufacturers. They also apply to food processing aids and also provide the prohibition regulation that no person can manufacture, import, export, distribute, advertise, display for sale or use any food additives, except food additives set out in the prescribed standards.

These regulations apply to all fortified foods manufactured, imported, exported, distributed, advertised, sold or used in Nigeria. The regulatory document provides for the advertisement of foods to which no vitamin and/or mineral has been added, label declaration of food to which vitamin and/or mineral has been added, a statement relating to the mineral content of food, label declaration of food mandatorily fortified with vitamin A, labelling, packaging, penalty and forfeiture after conviction.

These regulations apply to foods processed by ionizing radiation that is used in conjunction with applicable hygienic codes, food standards and transportation codes, manufactured, imported, exported, distributed, advertised, sold or used in Nigeria. The document provides information on the general requirement for food treatments, radiation sources, absorbed dose, facilities and control of the process, the wholesomeness of irradiated foods, packaging, quality assurance, inspection, re-irradiation, labelling, trade-in irradiated foods, importation, exportation, penalty, and forfeiture after conviction

These guidelines are for the interest of the general public and in particular, manufacturers of herbal remedies/dietary supplements made in Nigeria. The document emphasizes that no herbal remedies/dietary supplements shall be manufactured, imported, exported, advertised, sold, distributed or used in Nigeria unless it has been registered under the provisions of the National Agency for Food and Drug Administration and Control (NAFDAC) Act CAP N1 (LFN) 2004, other related Legislations and the accompanying guidelines.

This guideline is technically and structurally inspired by Health Canada’s guidance document on harmonized requirements for the licensing of vaccines and guidelines for the preparation of an application and the World Health Organization (WHO) working document on vaccine prequalification dossier. This guideline document has been developed in pursuance of the National Agency for Food and Drug Administration and Control (NAFDAC) Act Cap. N1, LFN 2014 and made to provide guidance to applicants on the organization of information to be provided to the agency in seeking marketing authorization for Vaccines for human use. The document applies to all vaccines to be authorized for human use, regardless of where they are manufactured.

The intention of this document is to provide acceptable principles for the registration of biosimilar products that are claimed to be similar to RBP of assured quality, safety, and efficacy that have been licensed based on a full registration dossier by a stringent regulatory authority. On the basis of proven similarity, the registration of a biosimilar will rely, in part, on non-clinical and clinical data generated with an already licensed RBP.

This document is for the interest of the general public and in particular, a non-governmental organization that wish to import NAFDAC regulated items. It emphasizes that no food, drug, cosmetics, packaged water, detergent, the medical device shall be manufactured, imported, exported, advertised, sold, 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 policy was designed to foster the integrated management of water resources for optimum, sustainable, efficient and equitable water resources development and management to meet the current and future user water demand, conserve the water quality and protect the environment. The specific objectives of the water resources policy are to optimize the use of the nation’s water resources at all times, to improve and expand the delivery of water services equitably, to prevent the over-exploitation of groundwater and protect its quality and facilitate the exchange of water sector information.