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Recent NAFDAC updates include a clarification on a previously issued alert, a blacklisting action against a pharmaceutical company, and guidance on handling manufacturer investigation reports for medical devices. These changes signal a heightened focus on regulatory compliance, product safety, and transparency in the health sector, with implications for manufacturers, importers, and distributors.
Pharmaceuticals
Medical Devices
Food Safety
Healthcare
International Trade
Regulatory Clarification on Deleject Disposable Needle Public Alert No. 042/2026
NAFDAC
NAFDAC clarified that the public alert regarding particulate matter in Deleject Disposable Needle Batch No. 240605 was uploaded in error, as the matter had been resolved after regulatory review.
Businesses dealing with medical devices should verify NAFDAC alerts and clarifications to avoid unnecessary product recalls or reputational damage.
2026 World Breastfeeding Week Capacity Building Event for Healthcare Professionals
NAFDAC
NAFDAC held a capacity building event for healthcare professionals as part of World Breastfeeding Week, emphasizing the importance of nutrition and food safety.
SMBs in the food and nutrition sector may need to align with NAFDAC's promotional and educational initiatives to enhance credibility and compliance.
NAFDAC joins the Federal Ministry of Health and Social Welfare, nutrition partners, and the global community in celebrating World Breastfeeding Week 2026
NAFDAC
NAFDAC celebrated World Breastfeeding Week, highlighting its commitment to promoting breastfeeding and ensuring the safety of breast milk substitutes.
Manufacturers of infant formula and related products should ensure compliance with NAFDAC regulations on marketing and labeling to avoid penalties.
Handling Manufacturer Investigation Reports for Medical Devices and IVDs
NAFDAC
NAFDAC issued guidance on the proper handling of Manufacturer Investigation Reports (MIRs) for medical devices and IVDs to ensure timely and effective risk assessment.
Medical device companies must establish robust procedures for managing MIRs to comply with NAFDAC expectations and maintain product safety.
Blacklisting of Onifam Laboratories Ltd
NAFDAC
NAFDAC blacklisted Onifam Laboratories Ltd and associated persons/entities from pharmaceutical business activities due to regulatory misrepresentation and improper use of approvals.
Pharmaceutical companies must ensure transparent regulatory practices; blacklisting can severely disrupt operations and supply chains.
SON rides on e-platform to facilitate international trade - Business News Nigeria
Other
SON is leveraging an electronic platform to streamline international trade processes, likely improving efficiency for exporters and importers.
SMBs involved in international trade should explore SON's e-platform to reduce delays and enhance compliance with standards.
How to Register Your Fish Farm with NEPC Nigeria: A Complete Export Guide - within nigeria
Other
A guide on registering fish farms with the Nigerian Export Promotion Council (NEPC) to facilitate export, covering steps and benefits.
Fish farmers and exporters should follow NEPC registration procedures to access export incentives and expand market reach.
Increased scrutiny on pharmaceutical and medical device compliance
Emphasis on product safety and quality assurance
Potential for stricter enforcement actions against non-compliance
Opportunities for digital trade facilitation via SON e-platform
Export growth potential in agriculture and aquaculture sectors
1
Review and update internal quality management systems to align with NAFDAC guidance on MIRs
2
Conduct thorough due diligence on regulatory partners and suppliers to avoid association with blacklisted entities
3
Monitor NAFDAC alerts and clarifications regularly to stay informed of regulatory changes
4
Engage with NAFDAC for capacity building and training opportunities to enhance compliance
5
For fish farmers, initiate NEPC registration to leverage export opportunities
6
Explore SON's e-platform for streamlined trade processes and ensure product standards compliance