NAFDAC registration

Who it’s for

Medical device manufacturers, importers, and regulatory teams preparing a Nigerian submission.

What we help you deliver

• Product classification and gap review
• Technical dossier preparation and coordination
• Local importer and licence-holder guidance
• Submission support and query-response coordination

Timing, with context

Scoping is agreed after document review. Regulatory review times depend on device class, dossier readiness, and the authority.

We agree responsibilities, milestones, and professional fees after reviewing your brief. Regulatory approvals and timelines are determined by the relevant authority.