Castor ePro is a clinical trial management software from Castor that facilitates data collection and patient engagement. It combines electronic data capture, real-time data monitoring, and patient randomization so researchers can effectively manage trial processes. Castor ePro supports mobile and web-based data entry, ensuring accessibility for participants, while also providing analytics tools to track trial progress. This software is designed to help clinical researchers improve data quality and improve participant experiences throughout the trial lifecycle. Key capabilities: electronic data capture real-time data monitoring patient randomization analytics tools reporting features Best for: clinical researchers that need to simplify trial data management and patient engagement.
Castor ePRO is a modern, patient-centered software designed to transform how clinical trial data is collected and managed. As part of Castor’s wider clinical trial suite, ePRO specializes in capturing patient-reported outcomes through digital tools, replacing outdated paper-based systems with an efficient and compliant solution. The software plays a critical role in supporting decentralized and hybrid clinical trials, where patient engagement and accurate self-reporting are essential. One of the standout aspects of Castor ePRO is its accessibility. Patients can use smartphones, tablets, or computers to log their symptoms, complete surveys, or respond to study questionnaires. Automated reminders ensure participants remain compliant with study schedules, minimizing missed data points. This feature alone significantly improves patient retention and data quality, two common challenges in clinical research. Castor ePRO also integrates seamlessly with Castor’s EDC platform, meaning that patient-reported data feeds directly into the electronic data capture system. This eliminates manual data entry, reduces errors, and accelerates analysis. For global studies, multilingual support ensures that trials can operate across multiple regions while remaining culturally and linguistically accessible to diverse patient groups.
Collects data directly from patients via secure digital forms.
Allows use on smartphones, tablets, and computers for patient convenience.
Sends automated alerts to patients for diary entries and surveys.
Fully compliant with FDA, EMA, and GCP standards for clinical data.
Connects with Castor EDC and other clinical trial systems.
Customizable patient questionnaires and symptom logs.
Patients can input data without internet access, syncing later.
Combines with Castor eConsent for smooth onboarding.
Clinicians can view and track patient-reported data instantly.
Secure export into clinical trial databases and analytics tools.
Designed for international trials with multiple languages.
Cloud-based system with GDPR and HIPAA compliance.
Role-based access for researchers, sponsors, and site staff.
Visual reporting to analyze trends and compliance rates.
Supports small single-site studies up to global multi-site trials.
Offers integration capabilities with external trial platforms.
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Castor ePro is a clinical trial management software from Castor that facilitates data collection and patient engagement. It combines electronic data capture, real-time data monitoring, and patient randomization so researchers can effectively manage trial processes. Castor ePro supports mobile and web-based data entry, ensuring accessibility for participants, while also providing analytics tools to track trial progress. This software is designed to help clinical researchers improve data quality and improve participant experiences throughout the trial lifecycle. Key capabilities: electronic data capture real-time data monitoring patient randomization analytics tools reporting features Best for: clinical researchers that need to simplify trial data management and patient engagement.
Does Castor ePro have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
0
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