With an ability to produce and supply wide variety of high quality medical products to the international market, Uzbekistan deserves to be a Pharmaceutical investment landscape for foreign drug makers. The Ministry of Health oversees product registrations and licensing in the region and mandates drug makers to be get necessary approvals before entering the market. Though the region seems to be lucrative for investments, the complex Regulatory regime might pose critical Regulatory procedural challenges for obtaining market authorizations.

Freyr, as a specialized Regulatory partner, assists foreign drug makers with a comprehensive suite of Regulatory Affairs consulting services to navigate the critical challenges in a streamlined manner. Freyr offers Regulatory services in Uzbekistan for:

  • Medical Devices
  • Pharmaceuticals
  • Veterinary

Freyr Offerings

  • Strategic Regulatory Consulting
  • Regulatory Affairs & Regulatory intelligence
  • Registration pathways and license management services
  • Market authorizations
  • Regulatory Submissions
  • CTD and eCTD application
  • Dossier Preparation
  • Pharmaceutical labeling and localization
  • Labeling and localization services

Freyr Advantages

  • Strategic and well-versed local regulatory knowledgebase – with M.O.H, Uzbekistan
  • 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