Overview

With a prosperous economy, Cyprus has become the most sought after destination for medicine and medical device manufacturers for investments in the region. To enter the region, manufacturers must obtain market authorizations from The Ministry of Health Pharmaceutical Services, an authority overseeing the registrations and licensing of the medicinal products in the region. Right from must-to-obtain CE marking for medical devices to successful product launch, foreign manufacturers might have to deal with the complexity of Regulatory procedures enroute accessing the market.

Freyr keeping abreast with the Cypriot Regulatory market updates, assists foreign manufacturers to navigate the Regulatory regime in the region with end-to-end Regulatory Affairs services. Freyr’s end-to-end Regulatory affairs consulting for Cyprus span across:

  • Medical Devices
  • Pharmaceuticals / Drugs
  • Cosmetics and Food Supplements
  • Biologics

Freyr Offerings

  • Strategic Regulatory Consulting
  • In-country representation 
  • Regulatory Affairs & Regulatory intelligence
  • Registration pathways and license management services
  • Dossier preparation, review and management
  • Regulatory Submissions
  • Labeling

Freyr Advantages

  • Strategic local Health Authority contacts – with Medical Device Regulatory Health Authority
  • 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