NAFDAC Registration & Regulatory Affairs (R & R) Directorate Guidelines for Renewal of certificate of registration for Imported Medical Devices in Nigeria
Ministry of Health, National Agency for Food and Drug Administration and Control, Nigeria
These guidelines are intended to provide guidance on the technical and other general data requirements when submitting an application for renewal of product licence for imported medical devices. It outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market.
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 ⬤
Contacts
Monica Eimunjeze
Director
National Agency for Food and Drug Administration and Control (NAFDAC)
Moji Adeyeye
Director General
National Agency for Food and Drug Administration and Control (NAFDAC)
Mahmuda Mamman
Permanent Secretary
Ministry of Health
Adeleke O. Mamora
Honourable Minister of State
Ministry of Health
Osagie Ehanire
Honourable Minister
Ministry of Health
Muhammadu Buhari
President of the Federal Republic of Nigeria
NAFDAC Registration & Regulatory Affairs (R & R) Directorate Guidelines for Renewal of certificate of registration for Imported Medical Devices in Nigeria Current Version
January 2022
These guidelines are intended to provide guidance on the technical and other general data requirements when submitting an application for renewal of product licence for imported medical devices. It outlines the process to be followed and the technical requirements to be met before a product can be placed on the Nigerian market.
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