1INPUTS
Signals + study intent
- Wearable sensors
- Participant context
- Protocol + rules
STARDEEP™ PLATFORM
Turn complex health data into intelligence designed for the edge.
StarDeep™ converts multimodal health data into compact on-device models; NeuTigers disease programs package those models into partner-ready solutions.
Request technical diligence →SYSTEM ARCHITECTURE
From signals to governed trial intelligence.
One accountable supervisor converts broad study intent into governed work, executed in parallel by small, fit-for-purpose agents.
2ORCHESTRATE
StarDeep™ Supervisor Agent
One accountable master converts broad intent into governed work
UNDERSTAND INTENTDECOMPOSE + ROUTEVERIFY + ESCALATESTITCH + REPORT
3EXECUTE IN PARALLEL
Specialist agent swarm
Small, fit-for-purpose agents do the work
Validate dataExtract featuresAnalyze locallyManage alertsSummarize + report
4OUTPUTS
Governed trial intelligence
- Study dashboards
- Clinical alerts
- Health summaries
- Audit-ready reports
GOVERNANCE FOUNDATIONLocal-first processingHumanity-in-the-loopPrivacy by designTraceable + auditable
AGENTIC AI
One AI manager runs the whole trial.
A single accountable supervisor plans, routes, monitors, verifies and integrates — with humans in the loop from day one to database lock.
24/7ONE ACCOUNTABLE SUPERVISORIntent → Decompose → Route → Verify → Escalate → ReportHUMAN-IN-THE-LOOP
1UNDERSTAND STUDY INTENT
- Protocol & eligibility rules
- Visit schedule / required data
- Safety and reporting rules
- Data-quality expectations
2DECOMPOSE & ROUTE
- Break broad intent into subtasks
- Select the best specialist agent
- Parallelize independent work
- Track dependencies & progress
3VERIFY AND ESCALATE
- Check every agent output
- Flag protocol deviations
- Escalate safety / quality issues
- Human review & immutable audit
4STITCH & REPORT
- Combine validated agent outputs
- Daily compliance digest / KRIs
- DSUR-ready safety inputs
- CSR + CDISC + eTMF at close
WATCH · OVERSIGHT→REPORTING · CONTINUOUS→CLOSE · FINAL
Supervisor reconstructs who did what, when — under which rule — inspectable from day one to database lock.
ICH-GCP E6(R3)FDA 21 CFR Part 11EU CTR 536/2014GDPR / HIPAAALCOA+
DECENTRALIZED TRIAL ENGINE
How the AI helpers watch over patients at home.
Six specialist helpers — supervised by the manager — turn everyday wearable data into checked, explained, actionable clinical signals.
PARTNER DELIVERABLES
One program, staged for decisions.
Feasibility: intended-use framing, data audit, device constraints and evidence hypothesis.
Development: model prototypes, optimization, evaluation plan and integration specification.
Validation: study support, data-quality controls, performance analysis and documented status.
Deployment: device integration support, workflow design, monitoring and lifecycle planning.
START A QUALIFIED DISCUSSION
Move from a strategic question to a defined feasibility path.
Tell us about your device, therapeutic program, clinical study or market opportunity.
Contact NeuTigers ↗