Clear-cut Regulatory guidelines coupled with constantly growing economy makes the United Arab Emirates (UAE) a favorable destination for foreign medicinal products & medical device manufacturers who are willing to enter the region. The Ministry of Health regulates the importation of medical devices and medicinal products. It can sometimes be difficult for foreign manufacturers to navigate through various Regulatory approvals required for importation which results in lengthy and complex procedural challenges.

To address the manufacturer’s unique challenges for UAE market access, Freyr provides knowledge-based Regulatory affairs in the region. Freyr, as a preferred global Regulatory partner, provides end-to-end Regulatory Affairs services to assist foreign manufacturers to minimize the compliance related risks in effective timelines to enter the UAE market. Freyr is capable to expedite the registrations and market approval processes for:

Freyr Offerings

  • Strategic Regulatory Consulting
  • Registrations and licensing
  • Dossier management
  • Pharmacovigilance
  • Regulatory roadmap for market access

Freyr Advantages

  • Strategic and well-versed local regulatory knowledgebase - with the Ministry of Health & Muncipality
  • 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