Overview

The growing number of foreign Pharma companies in Thailand coupled with the trend of regional harmonization forecasts a better business growth for the foreign imports of pharmaceutical products, devices, cosmetics, etc. Prior to importing or manufacturing in Thailand, manufacturers must obtain approval from the Food and Drug Administration of Thailand (Thai FDA). With the agency eyeing on the revised versions of regulations, anytime soon, foreign manufacturers might fall short of required Regulatory knowledge on new procedures necessary for market access.

Freyr, as a global Regulatory partner, assists manufacturers with expert Regulatory affairs in Thailand. To enable manufacturers, navigate through the Thai's regulatory system cost-effectively and in shorter timeframes, Freyr provides Regulatory consulting services for:

Freyr Offerings

  • Strategic Regulatory Consulting
  • Regulatory Affairs & Regulatory intelligence
  • Dossier management
  • Regulatory submissions
  • Pharmacovigilance

Freyr Advantages

  • Strategic and well-versed local regulatory knowledgebase – with Thai FDA
  • 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
Global HA Mandates
 
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