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Regulatory Submissions


The trialforce platform provides a fully integrated web-based regulatory submissions solution specifically designed for regulated Life Science eDMS and international eCTD submissions.

Key advantages:

  • Provides all standard international templates for regulatory submissions
  • Produces output in required format including eCTD and NeES
  • Validates output
  • Locking mechanism for Submissions
  • Provides 21 CRF Part 11 compliant audit-trail


Quick Contact Regulatory Submissions