CLINICAL TRIAL ADVERSE EVENT REPORTING SYSTEM

摘要

A system is provided that sends data to a safety compliance management system in response to an adverse event. The system receives a first event in response to a first interaction by a user, where the first event indicates that the adverse event is to be reported to the safety compliance management system. The system further receives a second event in response to a second interaction by the user, where the second event indicates that the adverse event is ready to be reported to the safety compliance management system. The system further collects data and sends the collected data to the safety compliance management system.