AutoCT
AutoCT reduces document prep from days to minutes. With AI-generated first drafts and effortless updates, it gives time back to regulatory teams. From CSRs and protocols to safety reports and IBs, AutoCT supports clinical development end-to-end—eliminating bottlenecks and accelerating submission timelines.
Clinical Study Report (CSR) Automation
Generate draft documents in minutes by automating the majority of content creation—starting directly from primary sources like protocols and TLFs.
Shape scientific narratives with AI-assisted content refinement—giving subject matter experts precise, sentence-level control to enhance clarity and nuance.
Verify content with sentence-level traceability back to source documents—accelerating reviews and reinforcing trust in your clinical trial report accuracy.
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Clinical Protocol Development
Generate complete protocol documents directly from your synopsis—no specific input format required—streamlining authoring while maintaining consistency.
Update protocol content as trial designs evolve—without manual rework or reformatting—supporting agility and reducing versioning friction.
Track every protocol update back to its origin—supporting clarity, alignment, and rapid iteration as your trial evolves.
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Safety Report Generation
Generate DSURs, SAE summaries, and safety reports rapidly and consistently—enabling dependable automation across all stages of safety reporting.
Maintain audit-ready safety documents with automatic version control and source traceability—ensuring consistency and global compliance.
Automate formatting and versioning to free pharmacovigilance teams—so they can focus on signal detection, safety strategy, and expert oversight.
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