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National Cancer Institute
U.S. National Institutes of Health www.cancer.gov
The caBIG program has been retired, and while this website is being maintained temporarily to prevent broken links and provide access to information on the subset of caBIG projects that were transitioned into the new NCIP program, it will be archived in the near future. For information on the NCI's biomedical informatics program, please visit http://ncip.nci.nih.gov.

The information and links on this website are no longer being updated and are provided for reference purposes only.

 

Adverse event reporting system (caAERS)

Collecting and reporting participant adverse events that occur during clinical trials can be easily accomplished using the Adverse Event Reporting System (caAERS). This application supports regulatory and protocol compliance for adverse event report and allows local collection, management, and querying of adverse event data, whether routine or serious. The built-in, configurable rules engine helps determine whether adverse events are serious or routine. It also supports service-based integration of data from other clinical trials management systems.

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The information and links on this website are no longer being updated and are provided for reference purposes only.