Secure Patient Data Collection Across Every Trial Site
Patient Data Collection Platform for CRO Research Operations
Gather, verify, and secure patient information efficiently during your entire clinical trial process with the help of our CRO Patient Data Collection Solution, providing researchers a framework for collecting accurate patient data from all sites and patients.
Why Use Our Platform?
Capture High-Quality Patient Data Across Every Site and Study Phase
The Patient Data Collection Platform offered by our company offers CROs an advanced system that ensures security, scalability, and validation for the process of capturing patient data throughout all phases of clinical trials and regardless of the type of sites involved as well as the mechanism for gathering patient data. This can include eCRF data, patient-reported outcome data, wearable data, remote monitoring data, and anything else involved in clinical trials.
Give every trial site and every data management team one trusted, validated platform for capturing patient data that meets the highest standards of quality, security, and regulatory compliance.
See Platform DocumentationFlexible Data Capture
Every Patient Data Type Captured in One Validated Environment
eCRF data, patient-reported outcomes, wearable feeds, and remote monitoring data captured and validated within one platform. Flexibility that accommodates every data collection method your trial requires.
This system is capable of handling case reports from data input electronically, collecting patient outcomes through patient-oriented portals, integrating remote and wearable device data, and uploading data directly from laboratories all in one CDISC-CDASH compliant database. Real-time data validation rules can be set up to detect errors at the point of data entry. This will minimize the number of queries required and help maintain data accuracy from the very first patient visit.
Explore Data Capture Capabilities
Site and System Integration
Connected to Every Site, System, and Data Source in Your Trial
Data flows from every site and every source into one platform automatically. Integration that eliminates manual data aggregation and keeps the full patient dataset current and complete.
The system supports the integration of the most prominent CTMSs, central labs, electronic patient reported outcomes systems, and regulatory data management systems via CDISC, HL7 FHIR, and RESTful APIs. With role-based access for each investigational site in place, all sites are capable of submitting information in a secure and governed environment.
View Site Integration DetailsData Quality and Compliance
Validated Data That Meets Regulatory Standards at Every Collection Point
High-quality data captured right the first time, at every site, across every visit. Data integrity controls that reduce query rates and keep every dataset regulatory submission-ready.
Data verification, discrepancy detection, e-audit trails, and electronic signatures that comply with the 21 CFR Part 11 guarantee that all patient data records are fully compliant with regulations regarding quality, integrity, and traceability, thus greatly decreasing the time spent locking the database and preparing data sets for regulatory purposes.
Learn About Data Quality Controls
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