Accelerate Regulatory Document Creation for Rapid Global Submissions
Transform Your Document Creation Process
Built on Microsoft’s architecture and infused with cutting-edge AI capabilities, Hyrding offers a transformational platform for Regulatory & Scientific Writing – reducing complexity, accelerating revenue timelines, and simplifying how distributed teams collaborate.
Save up to 50% Authoring Time
Dramatically reduce document creation time through intelligent automation and streamlined workflows
One Solution for All Document Types
Handle clinical, pre-clinical, CMC, and labeling documents within a single, integrated platform
Reduce Cycle Time Up to 30 Weeks
Accelerate end-to-end document lifecycle from initial drafting to final regulatory approval
The Hyrding Power Trio
Three core technologies working together for seamless document lifecycle management
Elemental Control
✓ Break down complex documents into manageable sub-units
✓ Assign and track each sub-unit via Hyrding applications
✓ Preserve integrity of the full document
✓ Real-time document viewing capabilities
✓ Patent-pending technology
Directed Artificial Intelligence
✓ Deploy AI Agents directly at the point of use
✓ Enhance content without losing control
✓ Tailored to your standards and templates
✓ Customer-centric AI configuration
✓ Seamless MS Word integration
Explicit Task Management
✓ Efficiently manage tasks with precision
✓ Real-time progress monitoring
✓ Track requirements, deadlines, and responsibilities
✓ Librarian, Shepherd, and User Dashboard apps
✓ Role-based access control