Your coordinators should spend time on patients, not paperwork

Trial operations run on retyping: activity logs, sponsor reports, invoices, EDC entry. We're building agents that do that work — with the hospitals that run the trials.

Every clinical trial requires data entry, tracking activities, compiling reports to the sponsor, preparing invoices. The work falls on coordinators retyping what's already in the system. We're teaching agents how to do all that work.

Built around how trial offices actually work

Nothing unbilled

Billable activity reconciled against protocol; every sponsor invoice completed on time.

Sponsor reports without the scramble

Activity formatted into the reports each sponsor requires, ready on schedule.

EDC always current

Source data entered once, queries cleared as they arrive — no re-entry backlog.

Coordinators back with patients

The paperwork goes to agents; the human work stays human.

Meet the
Clinical Trials Agents

Trial Activity Agent
Activity tracking per protocol, production verification, completeness checks
What they read

CTMS, hospital scheduling systems, trial protocols, activity logs

What they deliver

Activity verified against protocol, gaps flagged, trial status per study

Sponsor Reporting Agent
Activity formatting, sponsor-specific report preparation, submission tracking
What they read

Verified activity data, sponsor reporting requirements, trial documentation

What they deliver

Sponsor reports built to each sponsor's format, delivered on schedule

Sponsor Invoicing Agent
Billable activity reconciliation, invoice preparation, payment tracking
What they read

Trial agreements, activity records, billing schedules, payment statuses

What they deliver

Invoices reconciled to contracted rates, unbilled activity flagged, payments tracked

Regulatory Documentation Agent
Safety and adverse-event documentation, EU/EMA reporting preparation
What they read

Incident documentation, regulatory timelines, EMA reporting requirements

What they deliver

Safety documentation compiled and filed within regulatory timelines, full audit trail

The early program

We build each trial agent with a small group of hospitals — their workflows, their sponsors, their edge cases. Partners shape the agents learnings and go live first.

1

Week 1-3: Scoping

Working sessions with your trials office: your studies, sponsors, systems and volumes mapped.

2

Week 6-9: Co-Development

Agents configured on your real workflows; your team validates every output as it learns.

3

Week 9-12: Go Live

When an agent is production-ready, program partners get to deploy first

Trusted by leading hospital groups

Agents enable us to grow our capacity on demand, in a cost effective way . This new model changes the economics of running a hospital.

CFO, Ospedale Galeazzi
75%
Cases fully automated
90%
Reduction in DSO
Zero
Backlong remaining

"We're seeing a completely different way of working after only few months of deploying the agents - our teams and agents collaborate like colleagues"

Valeria Ingrosso
COO, Humanitas Research Hospital
Humanitas Research Hospital logo with IRCCS above the name.
4 Hospitals
Group deployment
99%
Success rate
500 Hours
Saved per month

No integration was required, the agent was trained to operate our systems like an employee: pulling data, checking numbers, and submitting  reports

Rui Gomes
CIO, ULS de Coimbra
16 hours
Saved per report
Integration
No APIs required
6 Weeks
time to go live

Hire your first agent

Close-up of a silver rectangular device with rounded corners and a carved circular logo in the center.