Life Sciences
Research Applications
Decentralized Trials
Enable remote vital signs collection without device logistics. Broader recruitment with lower operational burden.
Continuous Monitoring
High-frequency vital signs data between site visits. Capture more data points without participant burden.
Patient-Reported Outcomes
Combine subjective PROs with objective vital signs for richer outcome data.
Safety Monitoring
Remote safety surveillance with alerts for vital sign changes. Earlier detection of adverse events.
Real-World Evidence
Collect vital signs data in real-world settings for post-market studies and RWE generation.
Digital Endpoints
Explore vital sign-based digital endpoints as outcomes or companion measures.
Built for Clinical Research
EDC Integrations
We integrate with major Electronic Data Capture systems used in clinical research.
Exploring Contactless Vitals for Your Study?
Our research team can discuss protocol considerations, validation data, and integration requirements for your clinical trial.
Contact Research Team →Life Sciences FAQ
Common questions from pharmaceutical and research professionals
Is contactless vital signs technology validated for clinical research?
rPPG technology is an active area of published research with growing evidence across diverse populations. We can provide technical details and support your protocol development for regulatory submissions.
How does this help with decentralized clinical trials?
Participants can capture vital signs at home without shipped devices, reducing logistics burden and enabling broader geographic enrollment. Data flows directly to your clinical data management system.
What data formats do you support?
We support CDISC-compliant data export, HL7 FHIR, and custom formats. Data can be delivered via API, SFTP, or direct database integration with major EDC systems.
Can Circadify be used as an endpoint in trials?
Yes, our technology can support exploratory endpoints for vital sign-based outcomes. We recommend engaging with us early in protocol development to ensure appropriate validation and documentation.
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