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Clarivio
Dashboard prototype for the visual representation of cognitive diagnostics, biomarker tracking and clinical workflows. React-based, visually guided by publications such as SMC 2024 and NIA-AA 2024.
Prototype
Problem
Clinical diagnosis of cognitive deficits today relies on heterogeneous test forms, manual evaluation and distributed data sources — creating friction, inconsistencies and delayed diagnoses.
Solution
A React-based dashboard mockup that shows how standardised cognitive tests could be captured digitally, biomarker values integrated, and the clinical workflow from assessment to report represented in a structured way.
Target audience
A conceptual design for neurology practices, memory clinics and cognitive research groups in the German-speaking region — specialists who still largely rely on paper-based diagnostics.
Tech Stack
Compliance
Roadmap
Current state: Interactive frontend prototype with full assessment flow (CERAD-Plus, MMSE, MoCA, CDT), biomarker display (ATN cascade), MRI scoring, medication management, PDF report and role-based access control. Next steps: migration to TypeScript, backend integration with PostgreSQL, evaluation talks with a Swiss memory clinic, review of a FHIR interface for lab systems.
Guided by literature
The interface draws visual and structural inspiration from publicly available specialist literature and quality recommendations — including Swiss Memory Clinics 2024, NIA-AA 2024 Revised Criteria, CERAD-Plus (Memory Clinic Basel), Sperling 2024 on ARIA classification and the PRISCUS / FORTA lists for medication safety. This is a design-level reference, not a verified or validated implementation.
Screenshots
FAQ
Is Clarivio a medical device?
No. Clarivio is a design and frontend prototype without clinical validation and without certification. The system must not be used for diagnostics, therapy or patient care.
Can I test Clarivio in my practice?
The prototype can be demonstrated on request for portfolio and concept purposes. Productive use is not intended for regulatory and data-protection reasons — that would require a full MedDO/MDR approval review and a validated backend stack.
Is there a roadmap toward product readiness?
Next steps are migration to TypeScript, backend integration with PostgreSQL, evaluation talks with a Swiss memory clinic and review of a FHIR interface. Medical-device approval is not a current project goal.
Request a demo or partnership.
As a development project every integration is individual. Write to us and we will respond with a tailored assessment.