Lyfjaberg: resting-state EEG in adult assessment
Separately from the clinical record, we study resting-state EEG in adult assessment. The module is never required to create or sign a note.
In the Edda, Eir keeps company on Lyfjaberg, the hill of healing. We use the name for the research tier because it is a different place from the clinical record, and should look like one.
What we are building.
Eir Tech is developing a deterministic quantitative EEG calculator for a six-minute resting recording from a consumer-grade headband. It computes spectral measures and compares them with a normative reference. It is at technology readiness level 4, holds no regulatory approval and is never required to create or sign a note.
Phase 1 and Phase 2.
Phase 1 (platform validation on simulated cases) runs from December 2026. Phase 2 is a prospective clinical investigation planned from mid-2027, subject to MHRA notification and ethics approval. If you run adult ADHD assessments and want to help shape the workflow, we would like to speak with you.
Research is a separate choice.
The research module is separately permissioned, separately labelled and never required to create or sign a note. Eir does not submit your notes or audio to research. Participation is by agreement and is never a condition of any plan.
Opt-in contributions.
Clinicians can propose a limited aggregate contribution for internal review once they have at least twenty signed consultations. The proposal contains only a rounded count of signed consultations: no notes, audio, identifiers or EEG. Removing direct identifiers does not by itself establish anonymity, so any wider research dataset requires a reviewed protocol, a lawful basis, a disclosure-risk assessment and approval before release.
Work with us.
If you run adult ADHD assessments and want to help shape the Phase 1 workflow, or you have a research protocol or an evaluation partnership in mind, we would like to speak with you.
Relative band power, individual alpha frequency and signal quality for each channel. Measures only. No label, no threshold, no classification.
Research only · not a diagnostic tool. The module computes measures and compares them with a normative reference. It is not a validated diagnostic, treatment or emergency alert service.
Reach a signed, exported note on a synthetic case in your first ten minutes.
Start with a synthetic consultation today. Real-patient use begins only after your clinic's data agreement, configuration and access checks are complete.