Regulatory Services

Syncorp Health offers regulatory services across all phases of clinical development and device development.

We offer following services to our customers

  • Strategic regulatory advice for effective product development
  • Product development agency meetings with regulatory bodies such as DCGI, Korea-MFDS, AYUSH and FSSAI
  • Regulatory experts in developing approval strategies
  • Expedited programs, including Fast Track submission and approval
  • Post-filing support to provide complete response to regulatory inquiries

We offer a comprehensive portfolio of services which can be tailored to meet the customer needs
Clinical Operations Therapeutic Area of Experience Site Feasibility
Site Selection Study Startup Patient Recruitment
Site Services Project Management Site Monitoring
Data Management Biostatistics & Programming Medical Writing
Regulatory Services Safety Services Quality
Consulting Services Vendor Management Technology
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