Collect and see your data as it happens.
Capture enables researchers to vastly improve data quality and availability, and in turn, informed trial management. Clean data capture, guided and cleaned in the moment it happens – at the point of care using SureSource tablets – offers greater compliance with a conclusive audit trail for safer, more accurate clinical trials. Initially capture all your data electronically to advance the standard clinical trial process, reduce data entry error rates to nearly zero, trim time and cost, and provide immediate visibility into the status of the patient and the trial as a whole.
Better Protocol Execution
Better data starts with better protocol execution.
Capture enables the collection of source data and documents, error free, at the moment of patient interaction. Clean data capture – guided at the point of care – provides better quality data by improving compliance and providing a conclusive audit trail for safer, more accurate trials. By collecting both data and related source documentation, Capture uniquely facilitates remote and centralized monitoring. Making this data available the same day as the patient visit speeds the process and provides trial insights available with no other solution. Discover why the FDA and EMA promote and endorse eSource over EDC for better, faster, safer studies.
- eSource for sites. Designed to maximize data quality while reducing site effort, SureSource Capture collects and validates data during the patient visit. Designed to look and feel like paper source, Capture employs automatic data validations and logic checks to eliminate SDV, delivering quality data in minutes, not weeks. Because Capture delivers benefits to the site as well as sponsors, initial acceptance at sites vastly exceeds other clinical technologies.
- Unique technology integrations. Because Capture is used during the patient visit, it opens the door for unique and valuable integrations with other technologies. For example, Capture can eliminate paper-based supply management to maximize efficiency, transparency and compliance. Integrated with IVRS, Capture provides electronic management of clinical supplies at the subject, site and study level. Using bar code scanners, sites track receipt, assignment, return, and any changes to clinical trial supply for real time accountability. This provides better accountability and saves days of monotonous reconciliation effort at each site.
- Unique technology extensions or replacement. Collecting data at the moment it happens also opens the door for unique and valuable extensions or replacement of other technologies. Direct data capture replaces EDC and transforms RBM activities. Capture supports scales and assessments that can be used as a replacement for separate eCOA technologies at the site – unifying the data and simplifying contracting. Capture integrates with electronic informed consent solutions, again reducing complexity and supporting data integration and availability.