Nigeria - 2018 - Health

NAFDAC Registration & Regulatory Affairs (R & R) Directorate Guidelines for Registration of Drug Products Made in Nigeria

Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control, Nigeria

These guidelines are for the interest of the general public and in particular, manufacturers of Pharmaceuticals made in Nigeria. The document outlines guidelines for application for Registration of drugs made in Nigeria, issuance of notification and labelling of drugs made in Nigeria.

Process Flow

Department of Registration and Regulatory Affairs ⬤

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 ⬤

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NAFDAC Registration & Regulatory Affairs (R & R) Directorate Guidelines for Registration of Drug Products Made in Nigeria Current Version

January 2022

These guidelines are for the interest of the general public and in particular, manufacturers of Pharmaceuticals made in Nigeria. The document outlines guidelines for application for Registration of drugs made in Nigeria, issuance of notification and labelling of drugs made in Nigeria.

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