Overview

With Its rapidly growing economy, Nigeria has been a desirable emerging market for investors. With medical devices and pharmaceutical markets in Nigeria are expected to grow in coming years, foreign manufacturers shall consider quickly initiating their efforts for obtaining market access. Under the Nigerian Federal Ministry of Health, the National Agency for Food and Drugs Administration and Control (NAFDAC) and the Pharmaceutical Council of Nigeria oversees the drug and device regulations in the region. Though the market seems to be lucrative for imports, the regulations surrounded might pose a great challenge for manufacturers to navigate through.

Having a complete understanding of the Nigerian healthcare market and NAFDAC regulations, Freyr assists manufacturers to address the Regulatory procedural challenges cost-effectively and in a timely manner. Freyr’s Regulatory services in Nigeria span across:

  • Medical devices
  • Pharmaceuticals
  • OTC
  • Food and Food Supplements

Freyr Offerings

  • Strategic Regulatory Consulting
  • Regulatory roadmap for market access
  • Market Access licensing
  • Regulatory Affairs & Regulatory intelligence
  • Registration pathways and license management services
  • Marketing Authorization Applications, Post Marketing Maintenance
  • Quality Management Certification,
  • NAFDAC Product Registration
  • Good Manufacturing Practice (GMP) Audit

Freyr Advantages

  • Strategic local health authority contacts – with NAFDAC
  • Expert Regulatory team with proven global RA expertise
  • Proactive and Collaborative approach
  • Quick turnarounds and faster time-to-market
  • Keeping abreast with region-specific legislation and Regulatory guidelines