The Clinical Trial Database (CTDB) can help you manage data collection by automating the
processing and monitoring of data collection for research protocols. Through this user-friendly
interface, the CTDB helps facilitate the creation of forms, questions and intervals, and provides
a data entry component allowing for first- and second-key validation workflow. With the CTDB, you can:
Track clinical protocol data
Design data collection questionnaires
Capture data
Import and export data
Analyze clinical protocol data
Create reports
Other CTDB functionalities include:
System Administration feature: to control staff access to application and data
Multi-Sites functionality: with NIH as a coordinating center
Quality Assurance module: providing a workflow for third party monitoring
E-Regulatory Binder: a file management module for the regulatory documentation
Bio-specimen management module: Follows the NIH Bio-repository policy to track bio-specimens collected during trials
