Building the clinical workflow layer for long-duration EEG
NerveDX is an Iceland-based enterprise neuroinformatics company building the regulated workflow layer for long-duration clinical EEG: faster review, structured documentation, governed AI triage, and operational evidence for hospitals and partners.
Make expert EEG capacity go further
Continuous and long-duration EEG produce hours of data that must be reviewed by highly trained clinicians. NerveDX exists to help services prioritise attention, document findings consistently, shorten turnaround, and preserve the clinical accountability required for regulated care.
Our core project is product and workflow engineering around the complete lifecycle, not a stand-alone algorithm. AI triage is governed inside a platform that also handles review, human confirmation, reporting, integration, quality evidence, and audit.
Clinically useful, commercially credible
We connect EEG expertise, software engineering, quality management, and pilot measurement into a pathway that can support hospital adoption, partner validation, and commercial diligence.
Iceland parent. EU/EEA orientation. Nordic and European conversations first.
NerveDX is based in Reykjavík. We design for EU/EEA data-residency conversations and are seeking design partners across Iceland, the Nordics and the wider EEA - alongside the ICU/cEEG, EMU and neurophysiology services already described on this site.
Reykjavík · Iceland
Registered office of Taugagreining - NerveDX ehf.. Public contact: info@nervedx.ai.
EU / EEA deployment
Cloud region and residency are scoped per hospital. EU/EEA hosting and GDPR-oriented processing are core design assumptions - see Integrations.
Languages
This website is available in English, German, French, Spanish, Portuguese and Icelandic so buying committees can share pages internally. Language availability is not a claim that we are commercially live in every country.
A platform case for clinicians, partners and commercial teams
NerveDX is positioned around a clear health-system problem: scarce reviewer time, growing EEG volumes, and a need for governed AI that fits regulated clinical operations.
For clinicians
Prioritised review, qEEG navigation, structured reporting, and transparent model outputs designed to keep expert judgment in control.
For partners
Measurable collaboration milestones: prototype validation, pilot KPIs, regulatory readiness, integration planning, and clinical workflow evidence.
For commercial teams
A workflow platform with enterprise data architecture, defensible clinical evidence, and expansion paths across EEG settings.
Our principles
Workflow-centric
We build the process around the EEG, not a single detection step. Review, navigation, confirmation, reporting, integration and audit hang together.
Regulated from the start
Quality management, security and compliance are embedded in the architecture - so commercialisation isn't a redesign but a continuation.
Human judgment wins
AI augments attention. Clinicians confirm, correct and sign off. Provenance and documentation keep every decision accountable.
Complementary, not duplicative
Where research communities have strong EEG/AI expertise, we see partners. Our focus is the broader clinical workflow and commercialisation layer.
Enterprise-grade
Multi-tenant, secure, auditable and integration-ready - built to operate inside hospital infrastructure and regulated environments.
Measure the ROI
We validate reviewer time saved, turnaround, triage accuracy, report consistency and workflow efficiency with pilot KPIs, not just feature checklists.
What we intend to prove
NerveDX should be judged by whether it makes long-duration EEG services easier to operate safely. The project is therefore framed around practical evidence rather than broad AI claims.
- Reviewer time saved without removing clinical sign-off
- Shorter time from recording to actionable report
- More consistent annotations and reporting language
- Auditable provenance for every model output and human decision
- Deployment readiness for privacy-conscious hospital environments
Why this is credible
The work combines clinical need, software innovation, regulated product development and practical health-system value.
- Clear prototype-to-pilot milestones
- Measurable healthcare productivity outcomes
- Alignment with quality and regulatory pathways
- Partner-friendly architecture for research and clinical validation
Cross-functional expertise behind the platform
We are an Iceland-based company building capability across clinical workflow, platform engineering, quality and commercial operations - working with hospital and research partners internationally.
Technical & product
Platform architecture, browser-first clinical UX, high-performance EEG playback, secure multi-tenant services and integration APIs - from prototype hardening to pilot-ready workflows.
Clinical workflow & QA/QMS
Intended-use boundaries, EEG workflow design, usability priorities, annotation and reporting standards, plus quality-system evidence for regulated software.
Finance & operations
Funding accountability, operational planning, pilot onboarding and the commercial infrastructure behind sustainable hospital partnerships.
Regulatory & quality
ISO 13485-aligned QMS, risk management, validation evidence and MDR/FDA-aware software lifecycle practices.
Security & infrastructure
Hospital-grade security, privacy engineering, deployment architecture and operational resilience for regulated environments.
Partner & customer success
Clinical stakeholder communication, pilot measurement, partner collaboration and evidence that supports adoption decisions.
Help us build the workflow layer for long-duration EEG
We are actively recruiting specialists who care about clinical safety, auditable AI and hospital-grade software. If your discipline is below, we would like to hear from you - even if the exact title is not listed yet.
Platform engineering
Browser-first clinical UX, high-performance EEG playback, secure multi-tenant services and integration APIs.
Clinical & neurophysiology
EEG workflow expertise, pilot design, annotation/reporting standards and evidence that matters to services.
Regulatory & quality
ISO 13485-aligned QMS, risk management, validation evidence and MDR/FDA-aware software lifecycle practices.
Security & infrastructure
Hospital-grade security, privacy engineering, deployment architecture and operational resilience.
Customer & partner success
Pilot onboarding, clinical stakeholder communication and partner collaboration across health systems.
Your discipline
Convinced you can accelerate regulated EEG workflow adoption? Tell us how you would contribute.
We review every thoughtful introduction. Send a short note via our contact form with the subject “Team - [your discipline]”.
Let's talk
Whether you're an EEG service, a research partner or a commercial collaborator, we'd love to connect.