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NAFDAC has issued several updates including a clarification on a previously erroneous public alert, a blacklisting of a pharmaceutical company, and guidance on handling manufacturer investigation reports for medical devices. These actions underscore the agency's commitment to regulatory integrity and product safety, impacting pharmaceutical and medical device businesses. Additionally, NAFDAC's involvement in World Breastfeeding Week highlights ongoing public health initiatives, while SON's e-platform aims to facilitate international trade, benefiting exporters.
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 about particulate matter in Deleject Disposable Needle Batch No. 240605 was uploaded in error; the matter was previously investigated and resolved.
Businesses dealing with medical devices should note that NAFDAC's alerts may be subject to correction; they should verify official communications to avoid unnecessary product recalls or disruptions.
2026 World Breastfeeding Week Capacity Building Event for Healthcare Professionals
NAFDAC
NAFDAC hosted a capacity building event for healthcare professionals as part of World Breastfeeding Week, focusing on promoting breastfeeding and ensuring food safety and applied nutrition.
Healthcare providers and nutrition-related businesses may see increased emphasis on breastfeeding support and compliance with nutrition standards.
NAFDAC joins the Federal Ministry of Health and Social Welfare, nutrition partners, and the global community in celebrating World Breastfeeding Week 2026
NAFDAC
NAFDAC participated in World Breastfeeding Week 2026, reinforcing its commitment to maternal and child health and nutrition.
Businesses in the food and nutrition sector should align with public health campaigns and ensure products support breastfeeding practices.
Handling Manufacturer Investigation Reports for Medical Devices and IVDs
NAFDAC
NAFDAC provided guidance on handling Manufacturer Investigation Reports (MIRs) for medical devices and in vitro diagnostics, emphasizing their role in assessing complaints and adverse events.
Medical device manufacturers and importers must ensure robust procedures for creating and submitting MIRs to NAFDAC to maintain compliance and patient 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 adhere strictly to regulatory requirements; blacklisting can severely impact business 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.
Exporters and importers can expect more efficient procedures for standards compliance, potentially reducing delays and costs.
How to Register Your Fish Farm with NEPC Nigeria: A Complete Export Guide - within nigeria
Other
A guide on registering fish farms with NEPC for export purposes.
Fish farmers and exporters should follow NEPC registration requirements to access export markets and benefits.
Verify NAFDAC alerts before acting to avoid false alarms.
Ensure compliance with NAFDAC's MIR requirements for medical devices.
Avoid regulatory misrepresentation to prevent blacklisting.
Leverage SON's e-platform for faster trade facilitation.
Consider NEPC registration for fish export opportunities.
1
Review and update internal procedures for handling NAFDAC communications and alerts.
2
Implement robust systems for creating and submitting Manufacturer Investigation Reports.
3
Conduct internal audits to ensure all regulatory approvals are used correctly.
4
Register with SON's electronic platform for trade facilitation.
5
For fish farmers, initiate NEPC registration process to enable exports.