EIX-Preclinical Document Intelligence
Smart, compliant documentation for preclinical research and submissions
Freeing your experts to focus on innovation by streamlining documentation for speed and accuracy
Preclinical documentation is the foundation of successful regulatory submissions and clinical development. These complex documents, from preclinical study reports to investigator’s brochures, must meet strict standards with precision and alignment, while manual drafting is slow, resource-intensive and prone to errors.
Expert.ai’s EIX-Preclinical Document Intelligence streamlines preclinical report creation by transforming complex datasets into submission-ready documents. Combining generative and neuro-symbolic AI, it automates drafting, enforces consistency and ensures documents are aligned with source data and regulatory guidelines—saving time, reducing risks and accelerating submission readiness.
What it's for
Errors in preclinical documentation can delay submissions and increase regulatory risk. Manual drafting drains scientific and regulatory experts of valuable time. Scaling across studies and candidates demands consistency, while submission readiness hinges on accurate, audit-proof documents.
With EIX-Preclinical Insight, you can:
Generate submission-ready
Maintain consistency
Detect and correct
Collaborate efficiently
How it works
Our framework integrates hybrid AI approaches:
- Automated Drafting – Generates full scientific and regulatory documents from source data
- Neuro-Symbolic Reasoning – Ensure consistency and accuracy across outputs
- Generative AI – Produce high-quality narrative, tables and figures from multimodal inputs
- Adaptive Learning – Continuously improve with new data, report types and therapeutic contexts
Automated document generation
aligned with source materials
Built-in compliance
Ensure consistency and accuracy across outputs
Multilingual & multimodal content
generation (text, tables, figures)
Configurable framework
adaptable to therapeutic areas and report types
Secure, role-based access
to protect sensitive preclinical data
Benefits
Faster report drafting and submission preparation
Reduced regulatory risk through early error detection
Consistency across studies, reports and submissions
Cost savings and FTE efficiency gains
Stronger audit and inspection readiness
AI you can explain. Outcomes you can measure.
Let expert.ai show you how to apply AI—securely, transparently and at scale.
