Policies / Policies from 2018
Policies with publication year 2018.
Ministry of Health, National Agency for Food and Drug Administration and Control
These guidelines are for the interest of the general public and in particular, manufacturers of medical devices made in Nigeria.
Ministry of Health, National Agency for Food and Drug Administration and Control
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.
Ministry of Health, National Agency for Food and Drug Administration and Control
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.
Ministry of Health, National Agency for Food and Drug Administration and Control
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.
Ministry of Health, National Agency for Food and Drug Administration and Control
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.
Ministry of Health, National Agency for Food and Drug Administration and Control
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.
Ministry of Health, National Agency for Food and Drug Administration and Control
These guidelines are for the interest of the general public and in particular the Pharmaceutical Manufacturing companies in Nigeria. They prescribe the minimum requirements necessary for the issuance of authority to manufacture pharmaceutical products.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
The purpose of this guideline is to strengthen the NAFDAC system for effective post-marketing surveillance of medicines, and regulated products including medical devices to ensure that only quality and safe medicines and other regulated products are distributed throughout the country. The implementation of This guideline will enable NAFDAC to generate scientific evidence on the quality and safety of medicines and medical devices for improved health outcomes.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
These guidelines are for the interest of the general public and in particular, importers of narcotic and controlled substances into Nigeria. The document emphasizes that narcotics and controlled substances should not be imported without obtaining an import permit and permit to clear where applicable and the steps in this guideline should be followed when the Federal Ministry of Health (FMOH) awards a contract to any organization/company to import on its behalf.
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control
These guidelines are for the interest of the general public and in particular, importers of precursor chemicals into Nigeria. The document outlines the process for obtaining a permit to import precursor chemicals under the various international conventions and treaties and those controlled nationally.
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