BAA-Covered · GxP-Aligned · Human-in-the-Loop

Clinical Intelligence,
Automated.

Enterprise-grade AI that generates regulatory documents, profiles trial sponsors, and monitors compliance — all with 100% human sign-off on every output.

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Built for Clinical Research Teams

BAA Covered
GxP Aligned
Full Audit Trail
Human Sign-Off
Multi-Provider AI
Platform Capabilities

Three Engines. One Platform.

Purpose-built AI modules for the highest-impact workflows in clinical research operations.

Document Generator

Generate SOPs, monitoring visit reports, CAPA records, deviation reports, and 7 more document types from structured templates — QC-checked and audit-logged before human review.

11 Templates

Sponsor Intelligence

Automated profiling of clinical trial sponsors — pipeline analysis, site and investigator mapping, competitive landscape, and AI-enriched intelligence reports sourced from ClinicalTrials.gov.

Real-Time Data

Regulatory Intelligence

Continuous monitoring of MHRA, EMA, ICH, and HRA sources with AI-powered impact assessment. Automated alerts for guideline changes, safety signals, and regulatory updates.

5 Sources Monitored
10×
Faster Document Production
20+
API Endpoints
11
Document Templates
100%
Human Sign-Off

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The DEOX AI Platform is currently in closed preview with select clinical research teams. Join the waitlist to get priority access.

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