Who operates this site
Operator of this website, responsible for its content: Daniel Gruber. Contact: support@antevion.com.
- Operator
- Daniel Gruber
- Contact
- support@antevion.com
About Antevion
Antevion is the name of a software product in development, onboarding its first partner hospitals. Product examples on this site are illustrative and use fictitious data. No real patient data is processed before a signed data-processing agreement and a DPIA.
Intended purpose
Intended purpose. Antevion is administrative workflow software for hospitals. It records follow-up recommendations that clinicians have written in imaging reports, quoting the report text on which each record is based. It routes each recorded recommendation to the department that the hospital has configured as responsible for that type of finding, and assigns an owner.
It calculates due dates only from intervals stated by a clinician. Antevion never generates an interval. Where a recommendation states no interval, Antevion opens the follow-up recommendation immediately in the owning department as "no interval recorded" and, at the same time, asks the report author to state one. If the author has not answered within the number of days the hospital has configured, a named clinician in the owning department sets the interval. Where a recommendation lacks an action, Antevion asks the author to complete it.
Where the hospital enables it, Antevion also asks the report author to state whether follow-up is intended when a report mentions a finding type for which the hospital's reporting policy requires a follow-up statement and none was found.
Antevion identifies later scheduling events, namely a performed examination or an appointment of the kind the recommendation names, that may fulfil a recommendation, for staff to confirm. It sends messages to responsible staff and family doctors and, through the hospital's own channels and in wording approved by the hospital, to patients. It reports completion rates.
Antevion does not analyse images, assess the clinical significance of findings, generate or suggest clinical recommendations or intervals, estimate risk, prioritise patients on clinical criteria, monitor treatment, or propose treatment. All clinical decisions are made by clinicians.
Regulatory status
We do not yet have a written qualification opinion on Antevion under the EU Medical Device Regulation. Until we do, we make no claim about its status. We will obtain one before any pilot with real patient data.
Planned products
Planned products are plans, not current operations. Each will be subject to its own regulatory review before any pilot.
Sources
The figures quoted on this site come from published sources, listed in the Notes on the home page.
See the notesThird-party names and marks
Names of products, companies and publications mentioned belong to their owners.
Accessibility
Our aim is for this site to meet WCAG 2.2 level AA. If you find a barrier, write to support@antevion.com.
Credits
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