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EIX-Preclinical Document Intelligence

Smarter, faster, 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.

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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

preclinical reports directly from validated study data

Maintain consistency

across multiple study reports, protocols and dossiers

Detect and correct

errors early to reduce regulatory risk

Collaborate efficiently

with version control and transparency built in

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

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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.

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