Automated clinical trial oversight and execution

Phases deploys AI agents to oversee clinical trials, improving operational performance, data quality, and audit readiness by identifying risks and taking actions to solve issues.

Study 4421 · Phase IIIAgents running
TMF coverage6 zones
#3 Site live / enrollment345/706
#4 First monitoring visit9/14
#5 Significant study event90/214
#6 Annual IRB / IEC renewal11/14
#9 Close out monitoring57/137
#11 Ongoing190/746
AI actions0 today
Emailed site re GCP certification
Site 07 · Dr. Sarah Chen expiry flagged
2m agoTMF
Escalated liver enzyme findings
Multiple sites · Medical Monitor notified
4m agoUrgent
Chased unsigned consent form
Site 03 · patient 007 · auto-email sent
9m agoMVR
Monitoring visit report findings
Screening brain scan performed outside protocol window
Site 07
Issue
IRB approval status conflicts within ISF section
Site 05
PD
PI participation missing from attendee metadata
Site 02
Issue
Incorrect biopsy kit shipment to site
Site 11
Issue
Query management0 open
Site 03Weight missing, visit 3open
Site 07AE severity mismatchAI raised
Site 01BP value out of rangeresolved
Site 09Visit date transcription errorAI raised
Site 04Concomitant med uncodedcritical

Benefits

Study oversight that catches issues and takes action

One view of every site

See every site, region, and emerging risk in one place. AI agents read across your EDC, TMF, and CTMS, so issues surface the moment they appear, not at the next visit.

100% monitoring oversight, 94% faster

Our AI agent reviews 100% of monitoring visit reports in 94% less time than a human team, identifying emerging risks with 98%+ detection accuracy and resolving them before they cost six figures to fix.

* Benchmarked on synthetic data consisting of 5,000 monitoring reports, 70,000 study datapoints, and 5,000 TMF documents.

A TMF that stays audit-ready

AI keeps your TMF filed, QC’d, and inspection-ready automatically. No remediation sprints before inspection. No surprises at audit.

How it works

Works with the systems you already use

01Connect your systems

Connect to your trial systems including EDC, TMF, or CTMS, with or without an existing API.

02Deploy AI agents

AI agents monitor, analyze, and take action across your trial systems immediately.

03Automated oversight and action

Track every emerging issue and proposed action, and stay in control from one location.

Compliance

Certified for regulated research

HIPAA

BAA-ready controls for protected health information.

GDPR

EU privacy controls for regulated clinical data.

SOC 2 Type II

Enterprise-grade security, independently audited.

21 CFR Part 11

Audit trails and e-record controls for FDA-regulated work.

ICH GCP

GCP controls for governed clinical research workflows.

Security

Security that survives an audit

Dedicated, isolated environments

Each customer runs in its own isolated environment, so trial data stays separated from other customers instead of being mixed into a shared workspace.

Business continuity

Daily backups, multi-AZ recovery planning, and point-in-time recovery keep trial operations recoverable when infrastructure or data issues occur.

Human in the loop

Critical actions require explicit human approval, with an audit trail that shows who approved what and when.

Encrypted end to end

AES-256 encryption protects data at rest, and TLS protects data in transit between users, services, and integrations.

Your data stays yours

Your trial data is not used to train models. It remains your data, governed by the controls in place for your environment.

Team

Our team and advisors bring experience from

  • Roche logo
  • Genentech logo
  • Palantir logo
  • CSL logo
  • Allogene Therapeutics logo
  • Capgemini logo
  • Gilead logo
  • AbbVie logo
  • Meta logo
  • Nurix Therapeutics logo
Writing

From the blog

Our thinking on AI agents, security, and compliance in clinical trial operations.

View all posts

Q&A

Frequently asked questions

Put AI agents to work on your trial.

A short call with our team to discuss what a Phases rollout could look like for your trial.