Key Features/Benefits

Complies with CVMP and VICH reporting requirements

Provides full electronic reporting

VedDRA support

PSUR report preparation


As with human drug development, the safety of animals is a high concern for the major regulatory agencies.  As such there are also stringent rules for the collection and reporting of adverse event data and all veterinary drug manufacturers are required to comply.  The rules are also complex and recently they have been updated to support electronic reporting.

agVet™ – Veterinary Safety Reporting

agVet™ is a comprehensive veterinary safety reporting system that is compliant with the CVMP and VICH specifications.  Through agVet, veterinary drug manufacturers and collect, assess and report adverse events in accordance with the regulatory obligations.  With full electronic reporting, agVet offers an easy way to comply with the latest regulations.

Arisglobal agVet™


adverse event reporting software