Strategic Regulatory Partner for Success in Dominican Republic

  • Tailored Regulatory Support
  • Product Maintenance & Compliance
  • Flexible Regulatory Teams

Greetings from
Freyr Dominican Republic

Medicine and medical devices manufactures entering the State of Dominican Republic are required to get market authorizations from the Directorate General of Drugs & Pharmaceuticals, under the Ministry of Public Health and Social Assistance. Right from requiring an authorized representative to handling the Regulatory procedures for final approvals, manufacturers need a specialized focus on the region’s Regulatory regime for successful compliance.

Assisting manufacturers to navigate the complex Regulatory procedures, Freyr, as a specialized Global Regulatory partner, provides end-to-end Regulatory affairs consulting services for Dominican Republic. Freyr’s specialized Regulatory services for the region span across:

  • Medical Device
  • Drugs
  • OTC

Freyr Offerings

  • Strategic Regulatory Consulting
  • Regulatory roadmap for market access
  • Regulatory Affairs & Regulatory intelligence
  • Registration pathways and license management services
  • 510k files application

Freyr Advantages

  • Team with 25+ years of strong foothold in the region
  • Proven track record for device registrations and submissions
  • End-to-end cosmetic Regulatory consultation
  • Structured and cost-effective approach to ensure speed to market

Looking for Regulatory Support in Dominican Republic

Contact us now for Expert Guidance and Support