Approach
Agents do the manual work. People make the decisions.
We bring agentic AI to every process of a research site, so the routine work runs on its own and coordinators and investigators spend their time where it counts: with patients, on the science, and on the decisions.
What our agents take on
- Regulatory documents
- Filed, versioned and checked continuously.
- Scheduling
- Visits planned against each protocol's windows, with reminders sent to patients.
- Source data
- Captured once and checked as it is entered.
- Feasibility
- Answered from the site's real patients and capacity.
- Sponsor communication
- Tracked, answered and followed up.
People stay in charge
Agents prepare, check and follow up. People decide. Investigators make every clinical decision and remain responsible for each trial, as federal regulations require, and a qualified person approves every output that matters.
What it means
For sponsors: quick answers and the same standard at every site. For coordinators: more of the day with patients. For patients: clear scheduling and a team that has time for them.
Questions
Are you a CRO?
No. We operate research sites. Sponsors and CROs contract with our sites to run their studies.
Where do you operate?
We focus on independent research sites in the United States.
Do you replace coordinators or investigators with software?
No. AI agents take on the manual work so people can spend their time on patients, science and decisions.