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Enhancing Clinical Insights: Unveiling the Next-Generation ePRO Platform for Streamlined Patient-Reported Data in Clinical Research

ClinVigilant ePRO © (Electronic Patient-Reported Outcomes) platform is a state-of-the-art solution designed to optimize the collection and management of patient-reported data in clinical trials.

What Makes ClinVigilant Patient Engagement ePRO different from other solution provider?

Improved Data Quality

Improved Data Quality

Patient Engagement

Enhanced Patient Engagement

Regulatory Compliant
Cost Effective

Key Features of

Patient-Reported Data Collection
Facilitates the collection of data directly from patients regarding their health status, symptoms, treatment outcomes, and quality of life.
Real-Time Data Submission

Allows patients to submit data in real-time, often using mobile devices or web-based platforms, leading to more timely and accurate data capture.

Customizable Questionnaires

Offers the ability to create and customize questionnaires and surveys tailored to specific study requirements.

Symptom and Side-Effect Tracking

Enables patients to record and track symptoms and side effects, providing valuable insights into treatment efficacy and patient safety.

Reminders and Notifications

Sends automated reminders to patients to complete assessments, improving compliance and data consistency.

Data Visualization and Reporting

Provides tools for visualizing and analyzing patient-reported data, aiding in more informed decision-making.

Multilingual Support

Supports multiple languages to accommodate diverse patient populations.

Integration with Clinical Trial Systems

Integrates with other clinical trial systems like CTMS or EDC for seamless data flow and management.

Secure and Compliant Data Handling

Ensures data security and compliance with regulatory standards like HIPAA and GDPR.

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