In 2026, NAFDAC has introduced the ‘Reliance Guidelines,’ a transformative policy that accelerates the registration of drugs already approved by trusted regulators like the US FDA or EMA. However, the port clearance process remains the most rigorous in the logistics sector.
1. The NAFDAC Reliance Pathway
If your drug is approved by a recognized foreign authority, NAFDAC can now slash review times from 240 days to under 60 days. You must submit the original technical dossier and an e-NXP form. Check our NAFDAC Guide for more on this agency.
2. The 6-Month Shelf-Life Rule
As of March 2026, all imported medicinal products must have at least 6 months of shelf life remaining at the time of arrival at the Nigerian port. If your goods arrive with 5 months and 29 days, they will be slated for destruction by NAFDAC’s Ports Inspection Directorate (PID).
3. Mandatory PCN Licensing
The importer of record must be a licensed pharmacist or a company with a Pharmacist Council of Nigeria (PCN) superintendent pharmacist. You cannot process a Pharma Form M without a valid PCN premise license.
Conclusion
Pharmaceutical logistics is about ‘Cold Chain’ and ‘Compliance.’ For a look at the fees involved, see our NESS and NAFDAC Fee Guide.