Overview
From spirometry to cough monitoring, FeNO to eCOA — Strados delivers the full spectrum of respiratory measurement with continuous, real-world data between visits.
Every Strados endpoint is built on the same intelligence foundation: AI detection, expert annotation, and retained audio — the evidence standard that makes your data auditable from Phase I through Phase III.
Integrated Endpoint Suite
Next-generation, medical-grade technology designed to deliver the most accurate and patient-friendly respiratory monitoring available.
FDA Cleared · CE Mark
Air Next Spirometer
FDA 510(k) · CE Mark
RESP® Biosensor
Clinical Trial Ready
RESP® Watch
Point-of-Care
NObreath® FeNO
Software
eCOA
Endpoint suite
Patient Devices
Strados Cloud
Sponsor / CRO
Modular Capabilities
Each solution works independently or as part of the full suite. Configure the endpoint package that matches your study design.
Air Next
In-clinic and at-home pulmonary function testing with FDA-cleared portable spirometry.
RESP® Biosensor + Watch
Continuous, objective cough monitoring — wearable sensors that capture what clinic visits miss, in patients' real lives.
RESP® Biosensor
Acoustic lung sound analysis capturing wheeze, crackle, and other auscultatory signals continuously in real-world settings.
NObreath®
Point-of-care fractional exhaled nitric oxide measurement for airway inflammation assessment.
Electronic clinical outcome assessments and patient-reported outcomes integrated with objective data.
Integration Advantage
Fragmented vendors mean fragmented data. An integrated approach delivers better endpoints, faster.
Eliminate fragmented relationships. One contract, one data stream, one point of accountability across all respiratory endpoints.
Combine objective measurements with subjective outcomes for more robust, differentiated endpoint strategies.
FDA-cleared devices, validated algorithms, and GCP-compliant data handling designed for pivotal regulatory submissions.
Real-time data visibility and automated quality checks reduce query volume and accelerate database lock.
Full-Service Support
Strados delivers more than devices and data — we partner with you end-to-end to design, execute, and deliver high-quality respiratory endpoints.
Device provisioning, shipping, and returns managed across global trial sites. We coordinate the full supply chain — from kit assembly to site delivery — so your team doesn't have to.
Trained respiratory specialists review AI-detected events to ensure every data point meets the rigorous quality standards required for regulatory submissions.
We work with your clinical and regulatory teams to define endpoint strategies, prepare validation documentation, and align with FDA and EMA expectations.
Dedicated support teams provide training, troubleshooting, and ongoing assistance to sites and patients throughout the trial — reducing burden and improving compliance.
Built for Your Program
For Sponsors
Strados delivers every respiratory endpoint your program needs — cough monitoring, spirometry, FeNO, lung sound analysis, and eCOA — through a single specialist partner. One contract, one data stream, one point of accountability. Scientifically validated, GCP-compliant, and built for regulatory submission.
Design a StudyFor CROs
Strados is the single integration point for all respiratory endpoints in complex multi-modal programs. Complementary to — not competing with — your broader eClinical infrastructure. Phase I–III delivery experience across 34 countries, with full site support, device logistics, and GCP-compliant data.
Explore CRO PartnershipOur Collaborators
Tell us about your program and we'll help you design the right respiratory endpoint strategy.
Design a Study