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