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Pitt IACUC DLAR Adverse Event Reporting SOP and Form 2016-2025 free printable template

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ISSUE DATE: May 15, 2006, REVISION DATE: STANDARD OPERATING PROCEDUREADVERSE EVENT (AE) REPORTING IN ANIMALS USED IN BIOMEDICAL RESEARCH PROJECTS AT THE UNIVERSITY OF PITTSBURGH Approval(s): Director,
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How to fill out Pitt IACUC DLAR Adverse Event Reporting SOP

01
Identify the adverse event occurrence involving animal subjects.
02
Gather all relevant information regarding the event, including date, time, and details of the incident.
03
Fill out the required sections of the Pitt IACUC DLAR Adverse Event Reporting form thoroughly.
04
Describe the nature of the adverse event, specific animals involved, and any actions taken in response.
05
Include any potential impact on the research study and welfare of the animals.
06
Submit the completed form to the designated IACUC or DLAR office for review and follow-up.

Who needs Pitt IACUC DLAR Adverse Event Reporting SOP?

01
Researchers conducting animal studies at Pitt.
02
Veterinary staff involved in animal care and management.
03
Institutional Animal Care and Use Committee (IACUC) members.
04
Compliance and regulatory personnel overseeing animal welfare.
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The Pitt IACUC DLAR Adverse Event Reporting SOP is a standard operating procedure that outlines the process for reporting adverse events involving animal research at the University of Pittsburgh.
All researchers, faculty, and staff involved in animal research at the University of Pittsburgh are required to file the Pitt IACUC DLAR Adverse Event Reporting SOP when adverse events occur.
To fill out the Pitt IACUC DLAR Adverse Event Reporting SOP, follow the provided template, detailing the nature of the adverse event, contributing factors, and any actions taken.
The purpose of the Pitt IACUC DLAR Adverse Event Reporting SOP is to ensure the safety and welfare of research animals, to improve research practices, and to comply with regulatory requirements.
Information that must be reported includes the date and time of the incident, a description of the adverse event, affected animals, possible causes, and any corrective actions taken.
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