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
- Learn more about caDSR (no download - multiple links to access online tools on lower part of caDSR page)
Create standards-based electronic case report forms (e-CRFs) from common data elements
- Learn more about caDSR (no download - multiple links to access online tools on lower part of caDSR page)
Submit FDA 1572 investigator registration forms
Identify suitable clinical trials based on patient medical records and genetic profiles
- Learn about caMATCH
- Contact ncicb@pop.nci.nih.gov if interested in deploying caMATCH
Find existing common data elements or create/curate new ones
- Learn more about caDSR (no download - multiple links to access online tools on lower part of caDSR page)
Manage clinical trial participant information and scheduling
Manage documents related to study protocols in clinical trials
Register participants in single or multiple clinical trials
Track trial milestones for each participant
Receive notification of trial events
Collect and analyze data, report events from clinical trials
- Learn more about C3D
- Contact ncicb@pop.nci.nih.gov if interested in deploying C3D
Review clinical data from ongoing trials in real time
- Learn more about C3D
- Contact ncicb@pop.nci.nih.gov if interested in deploying C3D
Collect, process, and report participant adverse events, in compliance with reporting requirements