Clinical trial software, unified
The clinical trial platform that replaces the stack
eSource, EDC, CTMS, eRegulatory, ePRO, eConsent, safety, and participant payments on one audited data model. Capture study data once at the point of care and run everything else from it.
No payment details required. Designed for 21 CFR Part 11, HIPAA, and ICH GCP E6(R3).
Why research sites and sponsors switch
Research teams juggle separate eSource, EDC, CTMS, eRegulatory, and payment tools that do not talk to each other. Every gap between them is re-typed data, reconciliation work, and audit risk.
One data model, zero transcription
Sites capture source data once and sponsors review the same records. The eSource-to-EDC re-entry step, and every transcription error it creates, is gone.
Compliant by design
Append-only audit trails, versioned records, reason-for-change, and Part 11 signatures are built into the write path of every regulated record, not bolted on.
Operations that know the protocol
Scheduling, enrollment funnels, binders, and budgets all read the study definition, so status is computed from real data instead of re-typed into trackers.
Participants included
A native app for ePRO diaries, eConsent, visit reminders, and stipend balances, offline-capable with device capture times preserved as source data.
Money that reconciles itself
Completed visits accrue receivables and participant stipends automatically at the contract terms in force on the visit date.
Your data is yours
Open API, FHIR ingestion, ODM-XML migration in and out, and SDTM submission exports are included in every tier. No egress ransom.
Everything in the platform
Eleven modules, one definition of the study, one audit trail. Each capability reads and writes the same records, so nothing is synced, exported, or re-entered between them.
Study Definition & Build
Design the study once and every module runs from it.
Learn moreeSource / EDC
Capture once at the point of care. Review on the same record.
Learn moreePRO / eCOA
Participant-reported outcomes on the device already in their pocket.
Learn moreeConsent
Versioned consent with Part 11 signatures and automatic re-consent.
Learn moreCTMS
Site operations: scheduling, recruitment, enrollment, monitoring.
Learn moreeRegulatory
eISF binders tied to real roles, real documents, real expirations.
Learn moreSafety
AE to SAE to expedited report without leaving the dataset.
Learn moreFinancials & Payments
Budgets accrue themselves. Participants get paid the same day.
Learn moreAnalytics & Reporting
Dashboards per persona and a report builder over one model.
Learn moreInteroperability & Exports
FHIR in. CDISC out. An open API in between.
Learn morePlatform Administration & Compliance
Audited access control and a validation package per release.
Learn moreRun your next study on one platform
Start a 14-day free trial, no payment details required, or talk to us about your site's workflow first.