,Entering Nigeria’s pharmaceutical market offers vast opportunities, but navigating NAFDAC requirements, CTD expectations, and evolving Regulatory processes can be challenging without the right guidance.
In this short explainer video, we break down the essential steps you need for a seamless, compliant, and timely product registration in Nigeria—right from dossier preparation to final approval.
If you’re:
- Unsure how to begin your NAFDAC registration
- Struggling with CTD dossier compilation or Module 1 localization
- Concerned about Regulatory delays or incomplete submissions
This video provides a clear, simplified pathway that helps pharmaceutical companies avoid common pitfalls and accelerate approval timelines.
Watch our quick guide to understand how Freyr supports end-to-end registration—from dossier preparation and submissions to Regulatory follow-ups—ensuring your Nigeria market entry is smooth and hassle-free.
Watch now and connect with our experts to fast-track your NAFDAC approval.