Trials are delayed by software, not by science.
No patient is dosed until the study database is built and validated, and on every study that build is done by hand. We rebuilt the layer underneath so it is not.
Before a single patient is dosed, a data manager reads the protocol and hand-codes every case report form, every field rule and every edit check. On a mid-complexity study that is four to eight weeks. Almost none of it carries forward, because the next protocol is written differently.
Then the trial starts and the second cost arrives. Capture, randomisation, outcomes, coding and supply each sit with a different vendor on a different data model. Every pair between them is a connector to build, validate and reconcile — and every protocol amendment breaks one of them and freezes the rest.
Both look operational. Both are your data architecture. So we changed the architecture instead of adding features to work around it — every module reads and writes the same records, which leaves nothing to reconcile between them and nothing to migrate when the protocol changes.
Intelligence in every phase of the trial, on one platform.
The principles behind the platform.
One data model, or it does not ship
Every module earns its place on the same schema. We turn down features that would need a connector back to the rest of the product — those are precisely the features that create the problem we set out to remove.
The system proposes, a person signs
AI drafts forms, edit checks and queries. A qualified reviewer approves each one, and the full chain of proposal, review and approval is written to the audit trail. It is the only design that survives an inspection.
Compliance is architecture, not a feature
Audit trails, electronic signatures and record integrity are properties of the schema rather than a layer applied before a regulator visits. They cannot be switched off, because everything else is built on top of them.
A direct line to the team building it.
The fastest way to judge Trialion is a conversation with the people who build and validate it — no SDR queue, no qualification call. Meet the team.
We are hiring across clinical, engineering and quality.
5 open roles — for people who have run trials, and for people who want to build the software that trials run on.
See it on a protocol you are about to start.
Thirty minutes on the live platform, with the people who built it.