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Research

Adverse Event(s) and Reporting

Reporting significant and unanticipated adverse events (AEs) is essential to maintaining institutional credibility, fostering a culture of care, and ensuring animal welfare. Principal Investigators (PIs) are required to seek guidance from the Attending Veterinarian (AV) when adverse events occur. The AV will help assess the situation, seek resolutions, and assist in reporting when needed. 

Consultation with the AV is mandatory if: 

  • Pain or distress exceeds the approved animal use protocol. 
  • Intervention, such as administering analgesics, is not possible.

Completion of the Adverse Event Form is required to report any unforeseen or negative incidents affecting animals involved in research, testing, or educational activities. 

All animal deaths, whether reportable as an Adverse Event (AE) or not, MUST be reported to the Attending Veterinarian (AV), within 24 hours of notification of discovery. 

adverse event information

Commitment to Compliance and Care

By adhering to this policy, researchers demonstrate their dedication to the ethical treatment of animals, the integrity of their work, and the credibility of the institution. For guidance or further assistance, contact the Attending Veterinarian or IACUC Manager.