Clinical Trials, reimagined
AI-enabled, sponsor-sided clinical operations for UK biotech.
AI-enabled, sponsor-sided clinical operations for UK biotech.
The proposition
Hyper-fractional FTEs. Junior staff running your study. Cost overruns that drain capital from the science. DEOX exists to fix that.
2
Layers between you and delivery
45
SOPs in force
10×
Faster document production
100%
Human sign-off on every AI output
What we deliver
Everything you need to run a UK clinical programme — from site identification through to database lock. Specialist functions outsourced to best-in-class partners.
Programme Delivery
End-to-end project leadership. Senior CPMs engaged from protocol to closeout.
Quality
45+ SOPs, continuous compliance monitoring, inspection-ready at all times.
UK Operations
NHS, NIHR, and private research site network across the UK.
Regulatory
MHRA, HRA, and ethics committee submissions and ongoing intelligence.
Why DEOX
Every delivery decision framed from the sponsor's perspective — programme timelines, resource allocation, and risk tolerance aligned with your clinical development strategy, not a vendor9s margin targets.
What makes us differentNo hand-offs to junior layers after contract signature.
Two layers between you and delivery. Full GxP compliance.
10× faster document production. Enterprise AI with Business Associate Agreements — BAA-covered, SOC 2 certified, zero data retention.
NHS sites, NIHR infrastructure, UK-based investigators.
Quality system
A comprehensive QMS with 45+ SOPs, 19 process flowcharts, 39 operational tools, and AI-assisted compliance monitoring — powered by enterprise-grade, BAA-covered frontier AI with 100% human sign-off on every output.
45
Standard Operating Procedures
17
Process Flowcharts
39
Operational Tools & Forms
9
Company Policies
Discuss your programme fit, timeline, and how a leaner model delivers more.