Products
One core. One product in development, five planned.
Every Antevion product is designed on the same core: it quotes what a clinician wrote, gives it an owner and proves whether it happened. Imaging follow-up is the product in development. The others are planned on the same core, each with its own regulatory review.
Six products
The product family
- In development · onboarding its first partner hospitals
Imaging follow-up
Antevion
Designed to quote each follow-up recommendation in a signed imaging report and give it an owner and a due date. It starts with a leakage audit of the hospital's own reports.
Designed for Hospital boards, quality teams and owning departments
- Planned
Screening and suspected cancer
Antevion Pathways
After a positive screen or a written suspicion of cancer, Antevion Pathways will give each next step a named owner. Its suspicion clock will measure the time from the first sentence that raises the suspicion.
Designed for Health units and screening services
- Planned
All signed reports
Antevion Handover
Antevion Handover will quote the recommendations written in discharge letters and pathology reports, and hand each one to the family doctor or the owning team.
Designed for Hospital boards and quality teams
- Planned
Trial pre-screening
Antevion Research
Antevion Research will show a research centre the source sentences that may matter for an open trial. People will decide eligibility; no verdict, no ranking.
Designed for Clinical research centres and their coordinators
- Planned
Inherited cancer risk
Antevion Family
From a tumour report that suggests genetic testing, to genetics, to relatives tested: Antevion Family will give the referral an owner and count relatives tested per patient found.
Designed for Hospitals, genetics services and health units
- Planned
Evidence and trials
Antevion Observatory
With academic partners, Antevion Observatory will link what happened after each written recommendation to outcomes. At a later stage, it will support academic trials of follow-up intervals.
Designed for Academic partners, research funders and health authorities
Planned products are plans, not current operations. Each will be subject to its own regulatory review before any pilot.
In every product
Same core in every product: quotes the clinician, never generates an interval or a verdict; a person decides.
- Quotes the clinician's own words. Never paraphrases, never generates.
- Never generates an interval, a risk score or a verdict.
- A person decides every closure, every eligibility question and every handover.
- States its coverage and limits with every number.
- One installation per institution, designed to be hosted in the region its data-protection rules require.
It starts with one audit.
The leakage audit shows, from your hospital's own imaging reports, which recommended follow-ups have a matching later exam or appointment and which have none found. No change to anyone's workflow, and no patient contact.