The rapid economic growth coupled with domination of imported pharmaceuticals makes Cambodia a lucrative destination for foreign medicine and medical device manufacturers to invest in the region. The Ministry of Health, Cambodia and Department of Drugs and Food (DDF) oversees the drug regulations and registrations in the region. However, to navigate the Cambodian Regulatory regime manufacturers require expert Regulatory affairs for successful compliance and timely market authorizations.

Freyr, providing end-to-end Regulatory Affairs consulting services in the region, assists foreign manufacturers navigate the Cambodian Regulatory landscape in a streamlined and compliant manner. Right from Regulatory roadmap to documentation to submissions, Freyr’s Regulatory services in Cambodia span across:

  • Medical Devices
  • Pharmaceuticals / Drugs

Freyr Offerings

  • Strategic Regulatory Consulting
  • Regulatory roadmap for market access
  • Regulatory Affairs & Regulatory intelligence
  • Registration pathways and license management services
  • Marketing authorizations
  • Regulatory Submissions
  • Dossier Preparation

Freyr Advantages

  • Strategic and well-versed local regulatory knowledgebase – Drug Regulation Bureau (DDF)
  • 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