VivoSense
VivoSense specializes in providing scientific expertise and end-to-end services for the implementation of wearable and connected technologies in clinical trials. Their mission is to develop validated digital measures that improve decision-making and patient outcomes, leveraging digital health technologies and wearable sensors to transform clinical research and healthcare.
Industries
Nr. of Employees
small (1-50)
VivoSense
23 Corporate Plaza Drive, Newport Coast, CA 92660
Products
Wearable sensor data analysis platform (desktop and cloud)
Software platform for importing diverse device files, visualizing multiple physiologic channels, applying signal analytics (HRV, EMG, EDR, PPG, respiratory analysis), performing batch processing, and exporting study-level reports. Available with cloud hosting and trial-focused features.
Wearable sensor data analysis platform (desktop and cloud)
Software platform for importing diverse device files, visualizing multiple physiologic channels, applying signal analytics (HRV, EMG, EDR, PPG, respiratory analysis), performing batch processing, and exporting study-level reports. Available with cloud hosting and trial-focused features.
Services
Consulting and operational execution across trial design, sensor selection, device provisioning, data capture, preprocessing, analysis, and delivery of study-ready endpoints.
Managed pipelines for importing device files, preprocessing (including handling non-wear and missing data), automated quality control, and monitoring of data completeness and integrity.
Design and execution of analytical validation studies comparing wearable-derived metrics to clinical reference standards and algorithm performance testing in structured and free-living conditions.
Advisory services to align study hypotheses and participant burden with appropriate sensors, wear location, and data capture strategies.
Support for regulatory engagement, preparation of regulatory-ready datasets, and aligning evidence generation to FDA/EMA guidance and qualification pathways.
Design of participant-facing approaches for returning wearable-derived results, including opt-in choices, summarized reports, and semi-automated preparations to balance value with ethical considerations.
Consulting and operational execution across trial design, sensor selection, device provisioning, data capture, preprocessing, analysis, and delivery of study-ready endpoints.
Managed pipelines for importing device files, preprocessing (including handling non-wear and missing data), automated quality control, and monitoring of data completeness and integrity.
Design and execution of analytical validation studies comparing wearable-derived metrics to clinical reference standards and algorithm performance testing in structured and free-living conditions.
Advisory services to align study hypotheses and participant burden with appropriate sensors, wear location, and data capture strategies.
Support for regulatory engagement, preparation of regulatory-ready datasets, and aligning evidence generation to FDA/EMA guidance and qualification pathways.
Design of participant-facing approaches for returning wearable-derived results, including opt-in choices, summarized reports, and semi-automated preparations to balance value with ethical considerations.
Expertise Areas
- Digital biomarker development
- Wearable sensor analytics and signal processing
- Clinical trial integration of digital health technologies
- Data operations for wearable data (ingestion, cleaning, monitoring)
Key Technologies
- Wearable accelerometry / actigraphy
- ECG-derived respiration (EDR)
- Heart rate variability (HRV) analysis
- Electromyography (EMG) analysis