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2026-09-10

Regulatory Watch

AI-synthesized intelligence from CBN, FIRS, CAC, NAFDAC, SON, and NEPZA — so your business stays ahead of regulatory change.

September 10, 2026 6 updates 2 sources
NAFDAC is intensifying enforcement against substandard, falsified, and counterfeit regulated products while also mandating updated clinical trial training for stakeholders. For Nigerian SMBs in pharmaceuticals, healthcare, personal care, and retail, the immediate priority is supply-chain verification and regulatory compliance to avoid product seizures, blacklisting, and reputational damage.
What's being regulated
Pharmaceuticals and healthcare Personal care and cosmetics Retail and distribution (including PPMVs) Clinical research and trials Import and export trade Agro-processing and fisheries
Latest regulatory changes
NAFDAC and NHREC Announce New Dates for Mandatory Stakeholders Training on Clinical Trial Regulations in Nigeria
NAFDAC
NAFDAC and NHREC have rescheduled mandatory stakeholder training on clinical trial regulations in Nigeria.
SMBs involved in clinical trials, contract research, or health research must ensure staff attend the training to maintain compliance and avoid regulatory penalties.
Public Notice on Blacklisting Ayrtons Saunders Ltd, UK
NAFDAC
NAFDAC has blacklisted Ayrtons Saunders Ltd, UK, and its products, warning importers, distributors, and healthcare institutions.
SMBs importing or distributing products from this company must immediately stop and verify all UK-sourced pharmaceutical or related products to avoid seizure and sanctions.
Public Alert No. 043/2026 - NAFDAC Places Products Marketed by Mofus Nigeria Ltd on Watchlist
NAFDAC
NAFDAC has placed products marketed by Mofus Nigeria Ltd on a watchlist pending regulatory investigation.
Retailers, wholesalers, and PPMVs should quarantine or stop selling Mofus Nigeria Ltd products until NAFDAC concludes its investigation.
Public Alert No. 042/2026 - Seizure of Suspected Substandard and Falsified BPPL Artemether/Lumefantrine 80mg/480mg
NAFDAC
NAFDAC seized a suspected substandard and falsified antimalarial medicine, BPPL Artemether/Lumefantrine 80mg/480mg.
Pharmacy and medicine SMBs must check stock for this batch, remove it, and source antimalarials only from verified suppliers to protect patients and avoid liability.
Public Alert No. 041/2026 - Alert on Suspected Counterfeit ORACIRE+ Toothpaste
NAFDAC
NAFDAC alerted the public to counterfeit ORACIRE+ toothpaste being distributed under the guise of registered ORACARE+ toothpaste.
Retailers and distributors of oral care products must verify product authenticity, remove counterfeit stock, and educate staff on distinguishing genuine products.
How to Register Your Fish Farm with NEPC Nigeria: A Complete Export Guide
Other
A guide on registering fish farms with the Nigerian Export Promotion Council (NEPC) for export purposes.
Fish farming SMBs seeking export markets should register with NEPC to access export incentives, documentation, and market opportunities.
What this means for your business
NAFDAC is actively blacklisting and watchlisting companies and products, signaling stricter market surveillance.
Counterfeit and substandard products remain a major risk in pharmaceuticals, personal care, and consumer goods.
Mandatory training for clinical trials indicates tighter regulation of research and development activities.
Export-oriented SMBs in agriculture and fisheries are being encouraged to formalize through NEPC registration.
Supply chain transparency and traceability are becoming non-negotiable for regulated product SMBs.
What to do next
1 Immediately check inventory against NAFDAC alerts 041, 042, and 043/2026 and remove affected products.
2 Verify all suppliers and products against NAFDAC's registered products database before purchase or distribution.
3 Stop any dealings with Ayrtons Saunders Ltd, UK, and confirm no blacklisted products remain in stock.
4 Register for and attend the NAFDAC/NHREC mandatory clinical trial training if involved in clinical research.
5 For fish farm exporters, initiate NEPC registration and obtain necessary export documentation.
6 Maintain proper records of product sources and batch numbers to facilitate recalls or regulatory audits.
7 Subscribe to NAFDAC alerts and updates to stay informed of future regulatory actions.
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