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This form is used for submitting the first and second progress report of an approved animal protocol for research involving animal subjects at Fort Hays State University.
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How to fill out iacuc annual progress report

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How to fill out IACUC Annual Progress Report

01
Start with basic information: Title of the project, Principal Investigator (PI) name, and IACUC protocol number.
02
Provide a summary of the research conducted during the reporting period.
03
Include the number of animals used, sorted by species, and specify the justification for any increase in animal numbers if relevant.
04
Describe any changes to the approved IACUC protocol, including any modifications or unanticipated adverse events.
05
Report on the animal welfare considerations, including compliance with relevant regulations and institutional policies.
06
Detail any training or education provided to personnel involved in animal care and use.
07
Confirm that there have been no disciplinary actions, research suspensions, and any serious concerns raised regarding animal care.
08
Include a statement of availability for IACUC review if needed.

Who needs IACUC Annual Progress Report?

01
Researchers conducting animal studies that are subject to ethical oversight.
02
Institutions involved in research requiring compliance with federal regulations.
03
IACUC members who review and monitor animal research programs.
04
Funding agencies that may require annual reports for grant compliance.
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People Also Ask about

Before any use of the animals for the project begins. Investigators must receive IACUC (Institutional Animal Care and Use Committee) approval before starting any animal activities and procedures. This ensures that the proposed research is conducted ethically and in compliance with regulations and guidelines.
You should expect the Full Board process to take at least 1 month. Final Approval: You will need to wait until you receive an email containing the final approval letter before you can begin your research.
It varies. The length of time for review depends both on the IACUC and on the investigator. The IACUC reviewed 67 AUAFs in 2008 and 58 in 2007. The mean length of time from submission to approval for simpler protocols was 10-15 days; for more complex protocols, 30-45 days.
This committee review period is called Grace Period in the CATS IACUC system and lasts approximately 10 calendar days*. If a protocol is not called to Full Committee Review by any member of the IACUC during the Grace Period, the IACUC Chair assigns each protocol to a Designated Member Reviewer.
The IACUC conducts animal program reviews and facility inspections at least once every 6 months in ance with 9 CFR 2.31(c)(1-3).
has occurred, the IACUC Chair will formally notify the involved individual(s) in writing of the noncompliance violation and corrective actions. health or well-being of the animal(s), the IACUC can suspend the research or teaching activity. individual(s) must implement corrective actions. the corrective actions.

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The IACUC Annual Progress Report is a document submitted by researchers to an Institutional Animal Care and Use Committee (IACUC) to provide an update on the status of animal research projects and ensure compliance with ethical standards and regulations.
Researchers who are conducting animal research approved by an IACUC are required to file an Annual Progress Report to update the committee on their research activities and compliance.
To fill out the IACUC Annual Progress Report, researchers need to provide detailed information about the progress of their projects, including any changes to protocols, the number of animals used, and any adverse events. It usually involves completing a standardized form provided by the IACUC.
The purpose of the IACUC Annual Progress Report is to ensure that the research is conducted ethically, that animal welfare is maintained, and to update the committee on the progress of the research.
Information that must be reported on the IACUC Annual Progress Report includes the number of animals used, any changes to the research protocol, any serious adverse events, and a summary of the research findings or progress to date.
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