The Hyrding® Revolution in Life Sciences
Accelerate Regulatory Document Creation for Rapid FDA Approval
Save up to 50%
authoring time
One solution
for all regulatory document types
Reduce cycle time
up to 30 weeks end to end
Hyrding streamlines the creation of complex life sciences regulatory documents (including clinical, pre-clinical, CMC, and labeling) by coordinating company-wide contributions within integrated Microsoft tools. Harness the power of Elemental Control, Directed AI Agents, and Explicit Task Management for a seamless document lifecycle—from initial drafting to final approval.
Hyrding’s Power Trio
Elemental Control
- Break down complex documents into manageable parts.
- Assign and track each sub-unit via Hyrding applications while preserving the integrity of the full document.
Artificial Intelligence
- Deploy AI Agents directly at the point of use.
- Tailored to your standards and templates, Hyrding AI enhances content without losing control.
Explicit Task Management
- Efficiently manage tasks with precision using our Librarian, Shepherd, and User Dashboard apps.
- Track requirements, deadlines, and responsibilities in real time.