Sakura's agent stack automates the data-heavy, audit-critical work of running clinical trials — autofilling CRFs, citing sources to the exact line, matching patients continuously, and keeping every site monitor-ready. Click any agent below to watch it work on real study data.
Each agent works alongside a specific role at the site — CRC, CRA, PI, Regulatory Coordinator, Scheduler, Nurse — and all eight share the same structured patient timeline, executable protocol graph, and queryable regulatory state. Click any tab to see the agent in action.
Reads the patient's EHR note, reasons over the protocol's CRF schema, and populates every field with a confidence score and exact source citation — across any EDC, from any EHR.
Every CRF datapoint is linked to its exact EHR source — note ID, line number, author, signed timestamp. Part 11 compliant audit trail, always. Click any row to inspect the citation.
Continuously scans every new EHR encounter against every active protocol at your site. Detects newly eligible patients, re-verification events, and exclusion shifts — before the PI's next clinic.
Projects every scheduled visit against its protocol-mandated window and flags predicted conflicts before they become deviations. Suggests scheduling moves the coordinator can make with one click.
Reads the protocol, checks feasibility against your patient population, drafts site qualification documents, and assembles a regulatory binder — reducing typical startup time from 16 weeks to under 3.
Continuously scores your site's audit readiness across open queries, protocol deviations, regulatory doc completeness, and source verification coverage. Builds a prioritized punch list for every upcoming monitor visit.
The moment a patient is flagged eligible, this agent reaches out on their preferred channel — SMS, email, patient portal — answers their questions about the trial from the protocol's IRB-approved language, and books the screening visit directly into your practice management system.
The workflow that gates site capacity and trial revenue. Reads adverse event data from the EHR, codes it to MedDRA, evaluates SUSAR criteria against the Investigator's Brochure and patient history, then drafts the IND safety report — with a full justification trail for nurse, coordinator, and PI sign-off.
The agents aren't independent — they share a structured patient timeline, an executable protocol graph, and a queryable regulatory state. That's why a fix in one agent improves every other.
No rip-and-replace. Sakura reads from the systems your site already uses and structures the mess so agents can act on it.
Read-only by default. FHIR, HL7, and native APIs for the largest platforms in oncology and specialty trials.
Raw mess in, clean structure out — the only way agents can reliably act without hallucination.
We'll wire up a read-only connection to one study's EHR + EDC and run all eight agents against live data. You'll see results in under two weeks.
Leave your name and email and we'll reach out to schedule a 30-minute walkthrough on your site's data.