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Welcome to the Clinical Trial Database Web site.
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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:
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Track clinical protocol data
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Design data collection questionnaires
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Capture data
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Import and export data
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Analyze clinical protocol data
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Create reports
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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
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