Partner Programs

Add lung function
to every centre.

Offer the doctors who already refer to you a complete lung function service. Tests in your centres, reports signed centrally, results on one platform.

New test lineLung function on your menu
Central sign-offOne reviewer for many centres
Same dayReports back to referring doctors

The pathway

Walk in. Test.
Report the same day.

Your technicians run the tests. AI-assisted reports reach a pulmonologist for sign-off, then go straight to the referring doctor.

alveoflow Pro oscillometry station

Every patient can be tested.

Oscillometry needs only normal breathing, so no patient is turned away because they cannot do a forced blow.

Who runs it
Lab technician
Where
Centre testing room
Lab sees
Tests by centre and technician

Bundles

Two bundles. The full picture.

Spirometry and oscillometry answer different questions. Together they test every patient and catch what either test alone would miss.

alveoflow ProOscillometry (FOT)
alveoAir UltraSpirometry
alveoOxy6-minute walk test

Diagnose every patient, including those who cannot blow.

Spirometry is the guideline standard for confirming asthma and COPD. Oscillometry works with normal breathing, picks up small-airway disease early and tests patients who cannot do a forced blow. One visit, both answers, one report.

What the clinic can doLung Function BundleComplete Respiratory Bundle
Confirm asthma and COPD (guideline spirometry)IncludedIncluded
Test children, older adults and breathless patientsIncludedIncluded
Detect small-airway disease earlyIncludedIncluded
Bronchodilator response, both methodsIncludedIncluded
Exercise capacity and oxygen desaturationNot includedIncluded
COPD severity grading and rehab follow-upNot includedIncluded

Centre models

Match the bundle to the centre.

alveoConnect Flagship centreComplete bundle Collection centreLung Function bundle Home visitsPortable Neo kit

The full respiratory menu.

Large centres run the Complete Respiratory Bundle and become the referral point for the region.

  • alveoflow Pro, alveoAir Ultra and the walk test
  • Referral destination for nearby collection centres
  • Pulmonologist sign-off for the network

How a programme runs

From first centre to network in a quarter.

  1. Week 0Select centres

    Centres chosen on referral volume and space. Bundle matched to each.

  2. Week 1Install and train

    Devices installed, technicians trained and certified.

  3. Week 2Launch to doctors

    Referring doctors told about the new test line, with sample reports.

  4. MonthlyVolume review

    Busy centres add a second station. Quiet centres move to Neo.

  5. QuarterlyGrow the menu

    Walk tests and home visits added where demand shows.

Network dashboard

Every centre, every report.

Lab network overview, 24 centresIllustrative data
0Tests this month
0Reports signed
0Median minutes to report
0Referring doctors

Tests per centre per day

Baner11.2
Kothrud9.4
Wakad7.5
Hadapsar5.1
Chakan2.2

Network actions

  • Centre, BanerAdd second station
  • Centre, KothrudOn target
  • Technician refresherDue in 2 centres
  • Centre, ChakanMove to Neo

Commercial models

Grow the test line without the capital risk.

Rental

Monthly per station

A fixed monthly fee per station with support, training and replacement.

Per test

Pay per report

Pay for each report generated. Cost scales with your volume.

Purchase

Own the stations

Buy outright with an annual support and software plan.

Plan lung function for your network.

Tell us your centres and referral volumes. We will propose a bundle for each centre and a launch plan.

Design your programme
  1. Acquisition time of 15–30 seconds of tidal breathing per recording, from the alveoflow FOT System specification. Applies to alveoflow Pro and alveoflow Neo.
  2. FHIR R4 and HL7 v2 export from the alveoflow FOT System specification. ABDM integration supported.
  3. CDSCO Class B under MDR 2017. ISO 13485 and MDSAP as stated on alveo.fit. alveoflow: US 510(k) submission pending; not cleared for sale in the United States. alveoair is US FDA 510(k) cleared (K222525, August 2023).
  4. Screens show example data and do not represent a real patient. Interpretation is the responsibility of the treating clinician.