Solutions · For partners

Connected-respiratory intelligence, built into your product.

Build recorded inhaler-use and inhalation-technique data into your RPM, telehealth, telemedicine or digital therapeutics product without owning the device, algorithms and cloud underneath. Use the Respiro Connect SDK, REST APIs or a white-label route.

Device, app or data layer SDK, APIs & white-label Data platform Co-development support
Who builds with Amiko

For partners who need respiratory signal, not another hardware project.

The same platform can sit behind different partner models: a digital-health app, a digital therapeutic, a telehealth workflow, a connected-device programme or a branded respiratory experience.

Digital health

Apps and therapeutics

Add connected-inhaler data to a patient app, digital therapeutic, telehealth product or disease-management platform through SDK components and structured events.

Devices

Hardware and inhaler partners

Explore embedded or add-on sensing with Plastiape, including the manufacturing scope for your product.

Care platforms

Clinical and data systems

Bring objective dose-timing and technique data into your remote patient monitoring tools, telemedicine platforms, data warehouses or partner evidence pipelines.

The stack you skip

Three hard things, already solved.

Connected respiratory care is three deep problems stacked on top of each other: the sensor, the algorithms that read it, and the cloud it all runs on. We have spent years on all three, so you start from a foundation instead of a blank page.

Sensor hardware

Embedded or add-on modules across a wide range of inhalers, engineered with our manufacturing partner Plastiape to be cost-effective at scale.

Dose & technique algorithms

A data layer that turns raw signals into recorded inhaler-use timing and inhalation-technique information, not just a button-press log.

Data platform

Cloud infrastructure that supports the data and integration route for your product.

Integration options

Integrate at the depth that fits your product.

Take the data, embed the experience, or ship a finished app under your own brand. Three integration paths, one platform underneath.

One integration, the whole signal

Data you can actually build on.

Every integration path delivers the same processed, device-linked signal: inhalation-technique data beyond claims or self-report.

Structured, time-stamped and ready to surface in your own interface, clinician-facing view or data warehouse.

  • Recorded events. Device-recorded use timing and context.
  • Inhalation technique. Agree the technique information and context appropriate for your use case.
  • Usage trends. Decide how recorded use could be presented in your product.
  • Background sync. Sensor communication and data capture run quietly in the patient flow.
  • Webhooks & exports. Stream events in real time or pull structured reports.
The Amiko difference

You integrate one platform and inherit the whole stack: sensors, algorithms and a cloud platform, instead of stitching together three vendors and a compliance programme.

Integration plan

From first architecture review to live deployment.

A regulated integration needs more than endpoints. We map the use case, data contract, privacy boundary and launch path before code starts moving.

1 · Define the product job

Clarify whether Amiko is powering patient engagement, clinical monitoring, device connectivity, evidence generation or a branded respiratory programme.

2 · Scope data and boundaries

Choose API, SDK or white-label; define which data moves where; and agree how PHI, consent, residency and regulatory documentation are handled.

3 · Pilot, validate, scale

Test the agreed approach, learn from the first deployment and decide the next step together.

PHI-minimising by designSDK components can run without exposing patient identifiers, where the deployment allows.
Regional deployment pathsEU and US cloud options support data-residency and customer-policy requirements.
Regulatory documentationIntegration planning includes the evidence and documentation partners need for regulated markets.
Partner-owned experienceYou choose whether Amiko is visible, invisible or white-labelled in the user journey.
Trusted by design

Your users' data, protected by design.

Amiko is built under an ISO 13485:2016 quality system and delivered on secure cloud infrastructure, with GDPR- and HIPAA-aligned deployments, regional cloud options and documentation for EU MDR and US FDA pathways.

See quality & compliance

Plan the integration behind your respiratory product.

Tell us what you're building. We'll map the fastest safe path from Respiro Connect to your users.