NAFDAC Drug Evaluation & Research (DER) Directorate Guidelines for Production Inspection of Herbal Medicines and Nutraceuticals Manufacturing Facilities
Ministry of Health, National Agency for Food and Drug Administration and Control, Nigeria
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.
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 Production Inspection of Herbal Medicines and Nutraceuticals Manufacturing Facilities Current Version
January 2022
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.
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