Understand Trialion,
end to end.
The platform for running the data side of a clinical trial. These docs are written for the people who actually use it — coordinators, investigators, data managers, monitors, sponsors, and CROs — in plain language, describing the system exactly as it behaves.
Built to be understood
Documentation that teaches, not just describes
A reference a research nurse, a sponsor, a monitor, and an auditor can each read with confidence.
Plain language
Written for coordinators, investigators, data managers, monitors, and sponsors — not for engineers. The technical material has its own section.
Task-shaped
One page per role, one guide per job — enroll a participant, correct data, close a query, lock the database — in the order a study needs them.
Honest about gaps
Every regulatory control says what the software does and what remains yours. What is not built is listed in one place, not buried.
Generated where it matters
The role and permission tables come straight from the platform's own catalogue, so they cannot drift from what the system enforces.
Start where you are
Explore by who you are
Pick your perspective and follow a path built for it. Full role journeys live in Roles.
Learn by interacting
Interactive explorers for every system
Driven by the platform's real source data — so what you explore is what actually runs.
Regulated by design
Mapped to the standards that matter
Each framework has a dedicated page: the requirement, how Trialion satisfies it, current gaps, and the evidence.
The whole platform, in one guide
“How a trial runs in Trialion” tells the complete story — setting up, building a study, opening sites, enrolling, capturing data, cleaning it, signing, and locking the database — and links to a step-by-step guide at every stage.
Read the complete guide