Smart Alerts

Stay Informed and Stay Ahead with Smart Alerts

Welcome to the future of clinical trial management. Our innovative Smart Alerts feature redefines how researchers and healthcare professionals stay informed about patient-mediated data, ensuring timely intervention, proactive monitoring, and enhanced participant safety throughout the trial process. With Smart Alerts, you can harness the power of real-time data insights to optimize study outcomes and improve patient experiences.

Key Features of Our Smart Alerts System

  • Proactive Risk Management: Receive automated instant notifications of critical events or deviations in patient-mediated data, enabling swift intervention and proactive risk mitigation to safeguard participant safety and study integrity.

  • Adverse Events Notifications: Patients can quickly report adverse events for more timely surveillance and engagement.

  • Real-Time EHR Data Monitoring: Stay connected to participant data in real-time, allowing you to track key metrics, identify trends, and make informed decisions about study progression and protocol adjustments as needed.

  • Real-Time Patient Monitoring: Monitor patient-mediated data streams, including wearable device data, electronic diaries, and mobile health apps, in real-time to identify anomalies or deviations from expected patterns to quickly engage with your patient and mitigate risks quicker.

  • Customized Alert Parameters: Tailor alert parameters to match your study requirements and specific risk indicators, ensuring that you receive notifications that are relevant, actionable, and aligned with your study objectives.

  • Streamlined Communication: Facilitate seamless communication among research team members, healthcare providers, and participants, promoting collaboration and timely response to critical events.

  • Enhanced Participant Engagement: Demonstrate your commitment to participant welfare by leveraging Smart Alerts to proactively address concerns, provide timely feedback, and engage participants in their own care throughout the trial journey.

  • Multichannel Notification: Receive alerts via email, SMS, or within the clinical trial platform interface, allowing you to stay informed and take action wherever you are and whenever it’s needed.

  • Integration Capabilities: Integrate Smart Alerts with existing clinical trial platforms, electronic data capture (EDC) systems, and data management workflows, enhancing interoperability and data flow across the research ecosystem.

  • Secure, Bi-directional Communication with Patients: Easily connect with patients between study visits.

  • Collect Important Longitudinal Data: Patient Reported Outcomes and other questionnaires automatically presented to and collected from patients at designated time intervals.

Who Can Benefit?

  • Clinical Trial Sponsors and Investigators: Enhance study oversight, optimize protocol adherence, and mitigate risks through proactive monitoring and timely intervention.

  • Clinical Research Organizations (CROs): Improve operational efficiency, ensure data quality, and maintain compliance with regulatory requirements by leveraging Smart Alerts as part of your trial management strategy.

  • Healthcare Providers: Stay informed about patient status and treatment adherence, enabling proactive intervention and personalized care delivery to support patient outcomes.

  • Study Participants: Feel confident and supported throughout the trial process, knowing that your health data is being monitored proactively and that you will receive timely support and guidance if needed.