Review trial rules beside cited patient facts.
Code each eligibility criterion once, have a physician sign it, and keep patient facts beside their source citations. Built for oncology research teams.
Synthetic NSCLC pilot. No real patient records, no patient contact.
Built for the people who screen patients for trials
- Research coordinators
- Treating physicians
- Site administrators
Every criterion, in the protocol's own words.
Aramintas keeps the registry text beside the rule your team codes from it. Lines that cannot be coded stay as clinician judgement; nothing is dropped. Missing patient information stays visibly Unknown, never quietly treated as absent.
See how it worksFrom protocol to signed checklist
Four steps, each one recorded and audited.
- 01_Import
Pilot protocols arrive with their version history and registry status.
- 02_Code
Coordinators turn each eligibility line into a structured rule, or mark it for clinician judgement.
- 03_Sign
A physician reviews every rule beside the protocol text and signs that exact version. Signing a checklist does not establish any patient's eligibility.
- 04_Cite
Patient facts show their source document and clinical date where known. Missing information stays Unknown, and facts reported without a source are marked as such.
Inside the workspace
- Trial libraryPilot protocols, their versions and the selected site's checklist status.Available
- Coding and sign-offCoding queue, physician signing and amendment review.Available
- Patient factsSite roster, identity review and cited facts with corrections.Available
- Automated document processingReading uploaded records to propose patient facts.Not yet available
- Matching and referralsPatient-to-trial matching, referral approval and the referral board.Not yet available
