Overview
The integrated respiratory endpoint suite
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
The Strados Endpoint Suite
Next-generation, medical-grade technology designed to deliver the most accurate and patient-friendly respiratory monitoring available.
Endpoint suite
One suite. One data stream.
Patient Devices
- RESP® Biosensor
- RESP® Watch
- Air Next Spirometer
- NObreath® FeNO
- eCOA
Strados Cloud
- Automated QC
- AI Analysis
- Expert Overread
- Audit Trail
Sponsor / CRO
- Validated Data
- Real-time Dashboards
- Regulatory Alignment
Modular Capabilities
Deploy what you need
Each solution works independently or as part of the full suite. Configure the endpoint package that matches your study design.
Integration Advantage
Why one integrated suite matters
Fragmented vendors mean fragmented data. An integrated approach delivers better endpoints, faster.
Single Vendor, Unified Data
Eliminate fragmented relationships. One contract, one data stream, one point of accountability across all respiratory endpoints.
Stronger Endpoint Packages
Combine objective measurements with subjective outcomes for more robust, differentiated endpoint strategies.
Regulatory Confidence
FDA-cleared devices, validated algorithms, and GCP-compliant data handling designed for pivotal regulatory submissions.
Faster Time to Insight
Real-time data visibility and automated quality checks reduce query volume and accelerate database lock.
Full-Service Support
Complete clinical trial services
Strados delivers more than devices and data — we partner with you end-to-end to design, execute, and deliver high-quality respiratory endpoints.
Global Reach & Logistics
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.
- Multi-country deployment
- Device tracking & inventory
- Site onboarding support
Overread & Expert Review
Trained respiratory specialists review AI-detected events to ensure every data point meets the rigorous quality standards required for regulatory submissions.
- Human-in-the-loop validation
- Expert annotation of acoustic events
- Audit-ready quality records
Endpoint Validation & Regulatory Alignment
We work with your clinical and regulatory teams to define endpoint strategies, prepare validation documentation, and align with FDA and EMA expectations.
- Protocol endpoint design support
- Validation packages for submissions
- GCP-compliant data handling
Site & Patient Support
Dedicated support teams provide training, troubleshooting, and ongoing assistance to sites and patients throughout the trial — reducing burden and improving compliance.
- Site training & certification
- Patient helpdesk & tutorials
- Ongoing device support
Built for Your Program
Who we work with
For Sponsors
Comprehensive Endpoints. One relationship.
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
The respiratory specialist your sponsors are asking for.
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
Partners
Ready to design your respiratory study?
Tell us about your program and we'll help you design the right respiratory endpoint strategy.
Design a Study
