
Validation evidence a reviewer will accept.
In a regulated environment the run is not just a check. It is the record. Every step is timestamped, screenshotted and reproducible, which is what an auditor asks for.
Device displays and clinical desktop software are validated by hand because the interface is the only thing available to test against. That produces a signed checklist, not evidence — and a checklist cannot be replayed when a reviewer asks what actually happened.
70% time savedFICUS Health streamlined rehabilitation documentation with an agent that does the clicking.
Read the case studyOne system, three phases, and a document at the end of each.
Validation engineering and QA
Verification runs against the device display and the clinical workflow, with evidence attached.
ValidateRegulatory and quality affairs
Validation documentation produced from the run rather than written after it.
DocumentClinical operations and support
Recurring workflow checks and documentation on systems already in service.
OperateIf a person can operate it, the agent can.
Built for where it has to run.
See it on your own medical devices & health systems.
We scope the trial with you and run it on your real environment. A person answers, within one business day.