AI, automation and data for healthcare organizations
Practices, medical centres and clinics carry a large amount of work that is repetitive, documented and measurable. Nevraxia builds systems that absorb that work, and turns the resulting data into something a medical organization can act on.
What we build
- 01
Clinical report generation
Dictated or typed clinical notes are structured into a complete report, in the format your organization already uses, and reviewed and approved before it leaves the system.
- 02
Protocol libraries
Operative, interventional and endoscopic protocols shaped around your specialty and your own practice rather than a generic template — reviewed and approved by the organization, archived, and refined as they are used.
- 03
Process automation
Every organization has its own repetitive work: follow-ups, reminders, referral letters, internal summaries. We identify what can reasonably be automated, and automate that — not everything.
- 04
Patient-reported outcomes
Customizable QR-code collection of PROMs before and after treatment — pain, function, quality of life — together with the analysis that makes the data usable in a quality review.
- 05
Activity and economic analytics
Revenue, collections, backlog and receivables by physician, specialty and site, so a group practice can be run with the same visibility as any other organization of its size.
- 06
Clinical and surgical statistics
Complications, revisions, reinterventions and adverse events tracked continuously, rather than reconstructed once a year for a report.
Structured for European registries
Data captured in a structured way can be prepared for submission to European registries — SIRIS Spine, SIRIS Implant, Eurocrine, EPICARD, EPITHOR — and compared against national and European references. Registry connections are built per organization and per specialty, according to what each registry accepts.
- Capture designed around registry data models, so submission does not require a second round of manual entry.
- Comparison of your own indicators against published national and European references in your specialty.
- Detection of deviations from expected ranges, as an input to internal quality review rather than a verdict.
- What is submitted, in which form and on which legal basis is defined with your organization, in line with the GDPR and the Swiss Federal Act on Data Protection.
Scoped, built and priced per organization
- 01
Scoping
We start from what your organization actually does: volumes, specialties, existing software, and where time is currently lost.
- 02
Build
A first working scope is delivered and used in real conditions before it is extended. Nothing is built on the assumption that it will be adopted.
- 03
Operation
The system is maintained and extended as the organization changes. Training and support are part of the engagement, not an option.
There is no product catalogue and no per-seat price list. Scope, integration effort and the size of the organization determine the cost, and it is agreed before the work starts.
Start with a conversation
Whether you want to automate clinical work, have a product examined by a practising clinician, or bring a senior medical perspective into an engagement — a short first conversation is usually enough to establish whether there is something to do.