NAFDAC Registration & Regulatory Affairs (R & R) Directorate Guidelines for Registration of Medical Devices Made 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, manufacturers of medical devices 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 ⬤
NAFDAC Registration & Regulatory Affairs (R & R) Directorate Guidelines for Registration of Medical Devices Made in Nigeria Current Version
January 2022
These guidelines are for the interest of the general public and in particular, manufacturers of medical devices made in Nigeria.
Thank you for requesting an expert analysis
A member of our team will review your request and reply back to the email address on file.