Every night of sleep, read in full.

Somnalab takes a full overnight sleep study — dozens of PSG channels plus patient video — and returns an AASM-scored draft for your sleep physician to review, edit and sign.

Example hypnogram: wake, REM, N1, N2 and N3 across an eight-hour night

Illustrative hypnogram of one night. REM periods shown in pink.

Join the pilot waitlist See how it works

Built for the people who score sleep

A single study can take a trained technologist hours to score by hand. Somnalab does the first pass so your team can spend that time on review and on patients.

Upload what you already record

Standard EDF/EDF+ PSG files from your existing amplifiers, with synchronized patient video.

Scored to AASM rules

Sleep stages by 30-second epoch, arousals, respiratory events, limb movements and the summary indices your reports need.

Your physician stays in charge

Every automated score is a draft. Clinicians review, correct and sign off before anything reaches a report.

Runs where your data lives

Designed to run on a server inside your lab, so recordings and video don't have to leave your building.

From recording to signed report

  1. Upload the studyDrop in the overnight PSG file and video.
  2. Automatic scoringStages and events are scored epoch by epoch.
  3. Clinician reviewScroll the night, check flagged epochs, edit any score.
  4. ReportGenerate a report with hypnogram and sleep metrics.

Sleep is one part of a bigger picture

We're starting with the sleep study. Over time we want to bring in the other things that shape how you sleep.

Building now

Sleep study analysis

Automated scoring and review tools for sleep labs, developed under a medical-device quality system.

On our roadmap

Genetics

Genes linked to circadian rhythm and sleep timing, through accredited lab partners.

On our roadmap

Blood markers

Relevant lab results alongside sleep data, for your doctor to interpret.

Research preview: SomnoAtlas

The plan behind the product: a workbench that compares sleep-scoring algorithms across datasets, and the path to a regulated device. Draft documents with dummy data, no patient data.

Start here

Review pack

One page linking all three documents.

Open → Document

Product requirements

Full PRD v1.0: requirements, architecture, AASM rules, privacy and the SaMD pathway.

Read → Interactive

Compliance map

Follow one recording from lab to cleared device and see where DPDP, ISO and FDA apply.

Explore → Interactive

Algorithm atlas

Prototype workbench: algorithms, pipeline builder, a simulated night, benchmark matrix.

Try it →

Handled like the medical data it is

Privacy under India's DPDP Act

Consent-based processing, minimal data collection, and patient rights to access and erasure built into the product.

Quality system in progress

We are building our processes toward ISO 13485 for medical devices and ISO 14155 for clinical investigations.

Local-first by design

On-premise deployment keeps recordings inside the lab. Encryption at rest and in transit.

Join the pilot

We're looking for sleep labs and sleep physicians in India to help shape the first version.