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National Cancer Institute
U.S. National Institutes of Health www.cancer.gov
 

Clinical Trials Management

What would you like to do?

Organize and design clinical trials

Create, search, collect, and download common data elements for use in designing clinical data forms

Create standards-based electronic case report forms (e-CRFs) from common data elements

Submit FDA 1572 investigator registration forms

Identify suitable clinical trials based on patient medical records and genetic profiles

Find existing common data elements or create/curate new ones

Manage clinical trial participant information and scheduling

Manage documents related to study protocols in clinical trials

Register participants in single or multiple clinical trials

Integrate patient information and demographics with other applications in the caBIG® Clinical Trials Suite (CCTS)

Create, edit, and view study calendars for clinical trials participants and track activities as they occur

Track trial milestones for each participant

Receive notification of trial events

Collect and analyze data, report events from clinical trials

Collect clinical trials data (remote data capture) using electronic case report forms (e-CRFs) based on common data elements

Review clinical data from ongoing trials in real time

Query and view laboratory test results and send selected data to other applications in the caBIG® Clinical Trials Suite (CCTS)

Collect, process, and report participant adverse events, in compliance with reporting requirements

Provide summary reports to NCI Centers Branch