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Adverse event - An adverse event is any change in health that occurs in a person after he or she enrolls in a clinical trial. Not every adverse event is related to the treatment or test being studied, but researchers must report all adverse events to the Food and Drug Administration (FDA).
Vaccine Adverse Event Reporting System - The Vaccine Adverse Event Reporting System is a United States program for vaccine safety, co-sponsored by the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). VAERS is a post-marketing safety surveillance program, collecting information about adverse events (possible side effects) that occur after administration of vaccines.
Safety monitoring - Safety Monitoring of a clinical trial is conducted by an independent physician with relevant expertise. This is accomplished by review of Adverse events, immediately after they occur, with timely follow-up through resolution.
Safety barriers - Safety barriers are systems that stop or prevent adverse events from happening. They are normally used to mitigate the risk in an industrial system.
Source: BazSites.com
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