Winner — Mondaq Thought Leadership Award (2024, 2025 & 2026)
Food & Drug Administration (FDA) & NAFDAC Practice
Product Registration, CGMP Facility Audits, Product Recall Management & Life Sciences Due Diligence.
Product Approval & Market Authorization
Structuring statutory filing pathways to obtain product registration and import permits from NAFDAC and SON for food, pharmaceuticals, dietary supplements, cosmetics, and medical devices . We review product labels, health claims, and marketing materials for regulatory complianc
Facility Audits & Crisis Management
Preparing manufacturing facilities for regulatory inspections and Current Good Manufacturing Practices (CGMP) compliance . We handle responses to warning letters, manage product seizure investigations, and design product recall strategies during contamination incidents
Life Sciences M&A & Administrative Litigation
Conducting regulatory due diligence for corporate mergers, acquisitions, and licensing agreements involving pharmaceutical and food manufacturing assets . We represent clients in administrative hearings and judicial challenges against unlawful regulatory decisions
Registering A Product Or Facing A NAFDAC Compliance Audit?
Consult with our food, drug, and life sciences legal practitioners at Tafawa Balewa Square (TBS), Lagos Island