Regulatory
Compliance is a daily discipline — covering licensing, quality systems, and post-market safety.
NovaMed
Our regulatory commitment
NovaMed maintains robust systems aligned with NAFDAC expectations and international quality principles, including documentation discipline, validated processes, and continuous improvement.
NAFDAC compliance
NAFDAC compliance is embedded across our lifecycle: registration dossiers, inspections, batch release documentation, labeling control, and post-market commitments.
WHO standards
WHO-aligned standards influence our approach to quality risk management, supplier qualification, stability protocols, and pharmacovigilance readiness.
NovaMed
Certification grid
NAFDAC Manufacturing Licence
National Agency for Food and Drug Administration and Control
2025 • Manufacturing sites
ISO 9001:2015
International Organization for Standardization
2024 • Quality Management System
cGMP Compliance Programme
Internal + Regulatory Alignment
2025 • Production and QA/QC operations
SON Compliance
Standards Organisation of Nigeria
2023 • Standards alignment and quality
NovaMed
Downloads
Downloadable resources will be expanded as document management integration is added.
Pharmacovigilance
To report a suspected adverse event, contact medical@novamedpharma.com with product name, batch details (if available), and a clear description of the event.
Product recall policy
NovaMed follows standard pharmaceutical recall procedures: risk assessment, notification, product traceability, retrieval, root cause analysis, CAPA, and regulatory reporting as required.
NovaMed