https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cvm-gfi-117-vich-gl24-management-adverse-event-reports-aers
CVM GFI #117 (VICH GL24) Management of Adverse Event Reports (AER's) | FDA
This guidance document describes a system for the management of adverse drug event reports following the use of marketed veterinary medicinal products.