WebCRF allows for the complete integration of case report form (CRF) data. Data are available online, 24 hours a day, 7 days a week, increasing monitoring capabilities and allowing clinical trials to be completed
much more rapidly than with other data collection methods.
Selected Features:
- Uses the WebCRF Administrator Tool (WAT) to define and administer virtually any CRF
with full validation and informative flags (requires no custom programming)
- Uses WAT to manage sites and users
- Allows rapid set up (1-2 weeks)
- Integrates, manages, and views all clinical trial data with ultimate ease
- Generates multiple reports to follow study progress and metrics online
- Accesses study progress continually
- Displays all study data in one place online making it easier to stay up-to-date with study progress
- Allows data to be entered and validated, and databases to be locked, much more rapidly than with
other data capture methods
- Generates online queries and allows online data and study management
- Eliminates the need for virtually all manual double-entry
- Integrates with other CompleWare data capture tools
- Identifies potential problems early in the study
- Allows monitoring of the study to be done from anywhere that Web access is available
- Performs edit checks across tables (e.g. across all visits) so that plausibility checks are
integrated and real-time data validation occurs
- Allows multi-lingual data entry into a single database
- Provides extensive protocol specific portals
- Is unmatched in simplicity for users, while performing complex real time edit checks
- Uses CompleWare unified user log on
- Is compliant with 21 CFR Part 11 requirements for electronic records
WebCDL®
