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