Your full, end-to-end review flow, all through Aitrium.
Four steps, one system, in production today across academic and industry-sponsored radiotherapy trials.
Data Collection
Enroll sites and patients in minutes. Automated protocol ingestion reads the protocol and generates rich, patient-level collection schedules: study arms, regimens, and data requirements, without manual setup.
Distributed DICOM is gathered at each participating site, protocol-aware from the first upload. A typical upload is delivered in under two minutes, with validation built in, so fewer errors ever reach the trial.
Analysis & Aggregation
Standardization and automated QA scorecards turn raw plans into comparable, trial-level signal.
A wide range of insights is generated before any human opens a case, giving quality investigations a head start.
Review Workspace Automation
Adherence is enforced automatically: case deviations and issues are caught before they enter central review, which is where the 90% reduction in site back-and-forth comes from.
The reviewer's queue, triage, and routing are handled automatically, informed by the protocol.
Review Environment
A reviewer-grade DICOM annotation workspace, informed by the protocol and specialized for radiotherapy trials.
Reviewers see each case in the context of exactly what the protocol requires. The final read happens here.
Quality assurance that fits inside a trial budget.
Significantly more affordable than legacy central review, with the time savings to match.
1. Median 98 seconds start to finish, including user review; median active processing 41 seconds. 54 production submissions across 10 clinical institutions in 6 countries (March to July 2026), measured from platform audit telemetry.
Aitrium never receives your images: data moves over the secure channels your organizations already trust. Read how the data flows →
