eCOA and EDC Clinical Trials
eCOA and EDC Clinical Trials
eCOA and EDC Clinical Trials
Simplify and Accelerate Your Clinical Trials with Actuvi
Actuvi enables efficient, patient-focused clinical trials with excessive data collection, improved accuracy, and enhanced participant engagement, reducing study timelines.
Why leading researchers trust Actuvi
Why leading researchers trust Actuvi
Real-Time Data Collection
Capture patient-reported outcomes, physiological data, and clinical observations directly in the platform.
Real-Time Data Collection
Capture patient-reported outcomes, physiological data, and clinical observations directly in the platform.
Real-Time Data Collection
Capture patient-reported outcomes, physiological data, and clinical observations directly in the platform.
Real-Time Data Collection
Capture patient-reported outcomes, physiological data, and clinical observations directly in the platform.
Seamless EHR Integration
Easily pull real-world patient data into trial workflows with Actuvi’s seamless integration with major EHR platforms.
Seamless EHR Integration
Easily pull real-world patient data into trial workflows with Actuvi’s seamless integration with major EHR platforms.
Seamless EHR Integration
Easily pull real-world patient data into trial workflows with Actuvi’s seamless integration with major EHR platforms.
Seamless EHR Integration
Easily pull real-world patient data into trial workflows with Actuvi’s seamless integration with major EHR platforms.
End-to-End Trial Support
From eConsent to data collection and analysis, Actuvi offers an integrated platform to manage every step of your clinical trials.
End-to-End Trial Support
From eConsent to data collection and analysis, Actuvi offers an integrated platform to manage every step of your clinical trials.
End-to-End Trial Support
From eConsent to data collection and analysis, Actuvi offers an integrated platform to manage every step of your clinical trials.
End-to-End Trial Support
From eConsent to data collection and analysis, Actuvi offers an integrated platform to manage every step of your clinical trials.
Accelerated Study Timelines
Automate repetitive tasks like data entry and monitoring, reducing delays and improving trial efficiency.
Accelerated Study Timelines
Automate repetitive tasks like data entry and monitoring, reducing delays and improving trial efficiency.
Accelerated Study Timelines
Automate repetitive tasks like data entry and monitoring, reducing delays and improving trial efficiency.
Accelerated Study Timelines
Automate repetitive tasks like data entry and monitoring, reducing delays and improving trial efficiency.
Compliance and Security
Actuvi ensures your data meets HIPAA, GDPR, and GCP compliance standards for secure and reliable trials.
Compliance and Security
Actuvi ensures your data meets HIPAA, GDPR, and GCP compliance standards for secure and reliable trials.
Compliance and Security
Actuvi ensures your data meets HIPAA, GDPR, and GCP compliance standards for secure and reliable trials.
Compliance and Security
Actuvi ensures your data meets HIPAA, GDPR, and GCP compliance standards for secure and reliable trials.
Smarter Clinical Trials, Faster Results - Experience the Actuvi Advantage
Smarter Clinical Trials, Faster Results - Experience the Actuvi Advantage
Actuvi in Action
Actuvi in Action
Actuvi Advantage
Actuvi Advantage
Improve accuracy with real-time data capture and reduce manual entry errors
Improve accuracy with real-time data capture and reduce manual entry errors
Higher Data Quality
Higher Data Quality
Conduct trials of any size, from pilot studies to large-scale multicentre trials, without extensive IT support
Conduct trials of any size, from pilot studies to large-scale multicentre trials, without extensive IT support
Scalability
Scalability
Use Actuvi’s mobile-friendly tools to collect patient data from anywhere, ensuring participant engagement
Use Actuvi’s mobile-friendly tools to collect patient data from anywhere, ensuring participant engagement
Remote Trial Management
Remote Trial Management
Actuvi captures eCOA, eConsent, PROMs, PREMs and physiological data directly, eliminating the need for multiple tools
Actuvi captures eCOA, eConsent, PROMs, PREMs and physiological data directly, eliminating the need for multiple tools
Centralized Data Collection
Centralized Data Collection
Get instant visibility into patient adherence, dropout risks, and trial milestones with real-time dashboards
Get instant visibility into patient adherence, dropout risks, and trial milestones with real-time dashboards
Real-Time Monitoring
Real-Time Monitoring
Actuvi identifies gaps in compliance or critical metrics, helping researchers address issues before they impact results
Actuvi identifies gaps in compliance or critical metrics, helping researchers address issues before they impact results
Automated Alerts and Insights
Automated Alerts and Insights
Simplify Your Trial Workflow
Simplify Your Trial Workflow
Simplify Your Trial Workflow
Actuvi eliminates manual processes with automated data capture, task management, and reporting, enabling faster trial completion.
Simplify participant data entry and ensure compliance with medication schedules and trial protocols.
Engaged participants are more likely to complete the trial, reducing dropout rates and ensuring data completeness.
Save time and money by automating workflows and reducing trial timelines.
Address participant challenges early with Actuvi’s alerts, reducing dropout rates and ensuring data quality.
Improve trial outcomes with comprehensive, real-time data monitoring.
Ready to talk to our digital care expert to learn how you can accelerate clinical trials with Actuvi?
Ready to talk to our digital care expert to learn how you can accelerate clinical trials with Actuvi?
Ready to talk to our digital care expert to learn how you can accelerate clinical trials with Actuvi?
© 2025 Actuvi
© 2025 Actuvi
© 2025 Actuvi