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.

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

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 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 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.

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.

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.

This document proposes a strategic approach to increase accessibility to testing as new testing modalities are available and to complement Nigeria Center for Desktop Control’s work with donors, partners and the private sector to rapidly scale testing capacity to every state.

Pregnant women have a higher risk of severe illness when infected with viruses from the same family as COVID-19 and other viral respiratory infections, such as influenza. Therefore, this document provides guidelines for pregnant women and nursing mothers during the COVID-19 pandemic.

This memorandum explains the sections and terms in the 2014 National Health Act. The Act stipulates the regulation, development and management of a health system and sets standards for rendering health services in Nigeria.

The overall goal of this HIV/AIDS policy is to control the spread of HIV in Nigeria, to provide equitable care and support for those infected by HIV, and to mitigate its impact to the point where it is no longer of public health, social and economic concern, such that all Nigerians will be able to achieve socially and economically productive lives free of the disease and its effects.

The goal of this revised National Policy on HIV/AIDS is to control the spread of HIV/AIDS in Nigeria and mitigate its social and economic impact.

The overall goal of the National Child Health Policy is to ensure the survival and healthy growth and development of the Nigerian child. It covers newborns, under-five, and school-age children while adolescents are covered by other policies.

The overall goal of this national strategic framework is to reduce HIV/AIDS incidence and prevalence, provide equitable prevention, care, treatment, and support, and mitigate its impact among women, children, and other vulnerable groups and the general population in Nigeria by 25% by the Year 2009.

The goal of this policy is to promote and sustain equity, efficiency, accessibility, and quality in health care provisioning through collaborative relationships between the public and private sectors.