As a central location in the Middle East, Lebanon offers a good deal of business opportunities for the medical device manufacturers to enter the market and from there on to expand their strengths in the vicinities. The medical device market in Lebanon remains strong with major share of it coming through imports which forecasts a good future for manufacturers outside the region. Though the market seems to be lucrative, entering the region surpassing all the necessary regulatory requirements – registrations, compliance processes, and obtaining approvals - might lag manufacturer’s plans to market the medical devices in the shortest time possible.

Decoding all the regulatory requirements of the Ministry of Public Health (MOPH), Freyr navigates manufacturers through the necessary procedures for registering their:

  • Medical Devices (Class II and Class III – Generic and Innovators)
  • Pharmaceuticals / Drugs

Freyr Offerings

  • License Maintenance
  • Local Authorized Representation
  • Regulatory Documentation and Submissions
  • Device Registrations and Approvals
  • Regulatory Process Optimization
  • Regulatory Strategy Consulting

Freyr Advantages

  • Expert Regulatory team with 20+ years of experience
  • Cutting-edge updates of the region
  • Proactive and Collaborative approach
  • Quick turnarounds and faster time-to-market