Manage Lung Health from Hospital to Home
Who We Help
Hospitals + Health Systems
Skilled Nursing Facilities
Pharmaceutical Industry
Physicians + Group Practices
Payers + Payviders
Real-World Monitoring of Cough and Wheeze
As Featured In
The Award-Winning Remote Monitoring Technology Revolutionizing Lung Health
- ī¦Clinically Validated Data
- ļ¼Patient-Centered Design
- ī¬Machine Learning*
- gHistorical Biomarkers
- īÆWireless Data Transfer
The worldās only FDA-cleared device that is clinically validated to capture lung sounds including coughing, wheezing, rhonchi and other adventitious breathing sounds over time without requiring episodic patient intervention.
As demonstrated in a 2019 Strados-led study with NYC Health + Hospitals, the RESP Biosensor can be used continuously and has the ability to capture more complete respiratory data compared to intermittent monitoring using an electronic stethoscope.
*Machine learning algorithms and respiratory rate not cleared by FDA and for investigational use only
News & Resources
Unpacking the FDA Advisory Committee Meeting for Merck’s Gefapixant
In November 2023, Merck's chronic cough drug, gefapixant, faced a decisive setback from the FDA Advisory Committee. The concerns highlighted insufficient evidence for the drug providing a clinically meaningful benefit to adults with refractory chronic cough (RCC) or...
Beyond Cough Count: Why Itās Time to Go Deeper in Cough Trials
24-hour cough frequency has traditionally been recognized as the āgold standardā primary endpoint for indications such as refractory chronic cough, chronic bronchitis, and IPF-related cough. While frequency is undoubtedly a valuable metric to measure for cough, there...
Navigating the FDA Digital Health Technology Guidance: Insights for Respiratory Drug Developers
In December 2023, the FDA published its final release of "Digital Health Technologies for Remote Data Acquisition in Clinical Investigationsā a pivotal step in formalizing regulatory standards and guidance for remote data collection in clinical trials. As the FDA...
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