Nigeria - 2019 - Health

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 guide the technical and other general data requirements when applying for renewal of product licenses 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 ⬤

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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 guide the technical and other general data requirements when applying for renewal of product licenses 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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