Solutions · For partners

Connected-respiratory intelligence, built into your product.

Build objective inhaler adherence, inhalation-technique and respiratory-risk signals into your own RPM, telehealth, telemedicine or digital therapeutics product without owning the device, algorithm and regulated-cloud stack. Use the Respiro Connect SDK, REST APIs or a white-label route, and let Amiko run the sensors, algorithms and regulated cloud underneath.

Device, app or data layer SDK, APIs & white-label Regulated data infrastructure 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

Pair embedded or add-on sensing with a regulated data layer, from prototype fit to commercial-scale manufacturing with Plastiape.

Care platforms

Clinical and data systems

Bring adherence, technique and risk signals into remote patient monitoring dashboards, telemedicine tools, 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 regulated cloud it all runs on. We have spent years on all three, so you start from a validated, regulated foundation instead of a blank page.

Sensor hardware

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

Adherence & technique algorithms

A regulated medical-device data layer that turns raw signals into dose timing, inhalation-technique scoring and personalised breathing-risk: not just a button-press log.

Regulated data infrastructure

Secure, GDPR- and HIPAA-aligned cloud built under an ISO 13485 quality system: the compliance groundwork that takes years to lay, already in place.

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, with clear boundaries around device communication, data processing and regulatory responsibility.

One integration, the whole signal

Data you can actually build on.

Every integration path delivers the same processed, device-linked signal: the inhalation-quality data competitors can't get from claims or self-report.

Structured, time-stamped and ready to surface in your own interface, your clinician dashboard or your data warehouse, with deployment boundaries designed around your privacy and regulatory model.

  • Adherence events. Dose-level timing: scheduled vs. taken, captured on the device.
  • Inhalation-technique scoring. Objective quality of each actuation, not just a press.
  • Breathing-risk signals. Rising rescue-use and personalised risk, ready to act on.
  • 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 (medical-grade sensors, validated algorithms and a regulated cloud) 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

Build against Respiro Connect with Amiko support, run the first deployment, then scale the validated path to more users, inhalers or markets.

PHI-minimising by designWhere the deployment allows it, SDK components can operate without needing to expose unnecessary patient identifiers.
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. When you build on Amiko, that groundwork is already yours.

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.