Overview

With huge share of imports and certainly low volume of local manufacturing, the State of Kuwait portrays a better scope of foreign medical device and medicinal product manufacturers entering the market. While doing so, given the strong Pharma Regulatory structure of Kuwait, foreign manufacturers without a clear-cut market awareness might encounter procedural challenges to obtain licenses, registrations and product approvals from the State of Kuwait Drug and Food Control Administration.

With a dedicated regional delivery center in Dubai, Freyr is focused on navigating the clients throughout the market entry process. Right from providing expert Regulatory consultation on market requirements to defining foolproof Regulatory strategies to fetching out in-time Regulatory procedural support, Freyr’s Regulatory services for Kuwait span across:

  • Medical Devices
  • Drugs

Freyr Offerings

  • Strategic Regulatory Consulting
  • Regulatory Affairs & Regulatory intelligence
  • Dossier preparation
  • conversion of CTD to eCTD
  • Submission, maintenance and regulatory preparations as per GCC guidelines

Freyr Advantages

  • 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