Nigeria Medical Device Market Country Report

In order to gain market authorization for your medical device in Nigeria, you must register with the National Agency for Food and Drug Administration and Control (NAFDAC).

Let Emergo Group assist you in evaluating the Nigerian medical device regulatory framework as it applies to your device(s)

Emergo Group’s worldwide network of consultants as well as industry and regulatory sources enables us to provide in-depth analysis of medical device markets including Nigeria. Our Global Regulatory Overview reporting service for Nigeria covers:

  • Regulatory Background for NAFDAC
  • Product Assessment
  • Authorized Representation Issues in Nigeria
  • Medical Device Registration Requirements
  • Costs and Timeframes
  • Labeling and Language Requirements
  • Regulatory Roadmap for Nigeria

Please contact us for more information about our Regulatory Overview Report for Nigeria.