NAFDAC Drug Evaluation & Research (DER) Directorate Guidelines for Pre-Registration Inspection of Pharmaceutical Manufacturing Facilities in Nigeria
Ministry of Health, National Agency for Food and Drug Administration and Control, Nigeria
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.
Process Flow
Department of Drug Evaluation and Research ⬤
Office of the Director General NAFDAC ⬤
Office of the Permanent Secretary, Ministry of Health ⬤
Office of the Minister of State for Health ⬤
Office of the minister for health ⬤
Federal Executive Council ⬤
NAFDAC Drug Evaluation & Research (DER) Directorate Guidelines for Pre-Registration Inspection of Pharmaceutical Manufacturing Facilities in Nigeria Current Version
January 2022
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.
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