Knowledge Base for Precision
Curated reference documents. Generate full documents or individual sections at a time - giving you full control over AI-generated content, formatting, and flow.
VeriScribe™ Document Authoring Agent
Up to 60% faster document generation with Gen-AI powered efficiency — VeriScribe™.
Empower medical writers and study teams with intelligent automation that transforms how clinical trial documents are created, reviewed, and finalized.
The Future of Authoring Is Here
Writing protocols, SAPs, or CSRs shouldn’t take weeks. VeriScribeTM Document Authoring uses state-of-the-art LLMs to rapidly generate drafts aligned to your templates, references, and organizational standards - cutting authoring timelines by up to 60%.
Key Benefits
Faster
In minutes, VeriScribe™ generates document sections aligned with templates, style guides and references.
Smarter
Synthesizes vast amounts of information through an integrated knowledge base, Q&A chatbot, and TFL summarizations.
More Accurate
Built on decades of SME experience from Emmes Group, authoring hundreds of trial documents, generates robust content with inbuilt QC checks.
Collaborative
Enables human + AI collaboration and integrated multi-user Word document editing.
Product Features
AI Drafting Agent
Template-based content generation. Generate sections in minutes, iterate by giving the Drafting Agent additional instructions - powered by a library of agent skills and giving you control over outputs.
AI Quality Control Agent
Ensure quality from the start. Every AI draft runs behind-the-scenes quality checks, with the ability for a user to trigger additional document-level consistency checks.
Integrated Microsoft Word Workflow
Write, review and collaborate directly in Word. No more exporting or reformatting - your entire workflow now lives in a single environment. Tag collaborators, comment inline, track changes and finalize documents with full traceability.
One Solution for Documents Across the Study Lifecycle
VeriScribe™ currently supports document generation across protocols, statistical analysis plans, clinical study reports, and other core trial documents spanning the study lifecycle.
Document Authoring is already driving faster timelines and higher-quality outputs for our teams, and across Emmes' internal teams.
Let's Connect
Schedule a Meeting
Let's discuss how our document authoring expertise can support your next study.
- Speak with a document authoring expert
- Tailored solutions for your study needs
- Quick and easy scheduling
Resources
See VeriScribe™ in Action
Experience how AI can elevate your writing workflows - schedule a demo today.