Published evidence

Advancing the science of inhaled medicine.

This is Amiko's connected inhaler evidence library: peer-reviewed research, real-world evidence and RS01X validation from inhaler sensors that capture adherence and technique data others can't reach. Here's the published record.

Published & real-world evidence

Built on published science, run to medical-device standards.

Respiro's approach to connected respiratory care is grounded in years of peer-reviewed research and developed inside a certified quality system.

10+ Peer-reviewed publications & abstracts
40+ Commercial programmes & research studies
6,000+ Participants worldwide across studies & programmes
Respiro has been cited in
Chest European Respiratory Journal J. Aerosol Medicine & Pulmonary Drug Delivery Int. Journal of COPD Advanced Drug Delivery Reviews Therapeutic Advances in Respiratory Disease Pharmaceutics Chronic Respiratory Disease Respiratory Medicine

A selection of our published research is listed below.

Selected publications

Respiro in the literature.

A selection of independent and collaborative connected inhaler studies that put Respiro and the RS01X to use: from device validation to medication adherence, inhaler technique and real-world asthma and COPD care.

Peer-reviewed journal articles, conference abstracts/proceedings and industry features in which Respiro or RS01X was used or described. Conference items are abstracts or proceedings, not full peer-reviewed papers. A fuller bibliography is available to research partners on request.

For researchers

Put this evidence to work in your own study.

The literature above comes from work with academic and clinical partners. If you're designing a study, generating real-world evidence or validating a connected therapy, Respiro gives you device-linked data and a regulated platform to run it on.

Research with Respiro
  • Device-linked datasets. Dose timing and inhalation-quality signals from real-world use.
  • Study support. From protocol design to data export, on a platform built for regulated work.
  • Regulated data platform. GDPR-aligned, ISO 13485 quality system, with data-residency options.
Rigour by design

Research-grade because it's built to medical-device standards.

ISO 13485:2016Medical-device quality management
CE · EU MDRConformity under the Medical Device Regulation
GDPREU data protection by design
HIPAA-readyUS deployments, with BAAs available

Certification and regulatory scope vary by product and market. See quality & compliance →

Want to put this evidence to work?

Whether you're running an investigator-led study or an industry-sponsored trial, Respiro gives you device-linked data and a regulated platform to generate evidence on.