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IRB use only Form RA108 (Rev. 6×08) THE UNIVERSITY OF MONTANAMISSOULA INSTITUTIONAL REVIEW BOARD (IRB) CHECKLIST / APPLICATION (Use for Human Subject Research) Protocol No: Approval Date: Expiration
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01
Start by carefully reviewing the instructions provided by the university's institutional review board (IRB). These instructions will guide you through the checklist and ensure that you provide all the necessary information.
02
Begin by providing basic information about your study, such as the title, investigator's name, and contact information. Make sure to include any applicable study identification numbers.
03
Next, indicate the type of review your study requires. This may vary depending on the nature of your research and the potential risk to participants. Common options include exempt, expedited, and full board review.
04
Provide a detailed description of your study, including the research question, objectives, methodology, and expected outcomes. Be clear and concise, but ensure that you include all pertinent information.
05
If your study involves human participants, indicate how you will ensure their protection and obtain informed consent. Describe any potential risks and benefits, steps taken to minimize risk, and procedures for obtaining consent.
06
If your study involves the use of animals or other living organisms, provide information on how you will ensure their care and welfare. Specify any potential harm that may occur and the measures in place to mitigate it.
07
Consider any additional requirements specific to your university or discipline. This may include detailed information on data management, confidentiality, conflicts of interest, or funding sources.
08
Once you have completed the checklist, review it carefully to ensure all sections have been addressed and all necessary documentation has been attached. Double-check for accuracy and completeness before submitting it to the IRB for review.

Who needs irb checklists - university?

01
Researchers conducting studies involving human participants or animals need IRB checklists at the university level. These checklists help ensure that researchers are following ethical guidelines and protecting the rights and welfare of participants or animals involved in their studies.
02
University administrators and IRB members also require IRB checklists to review and assess the research activities conducted by researchers. They use these checklists to ensure compliance with institutional policies, federal regulations, and ethical principles.
03
In some cases, research sponsors or funding agencies may also require researchers to complete IRB checklists as part of their grant or funding application process. This is to demonstrate that the proposed research meets ethical standards and safeguards the interests of the participants or animals involved.
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IRB checklists for universities are tools used to ensure that research projects involving human subjects are compliant with ethical standards and regulations.
Researchers, faculty members, and students conducting research involving human subjects at universities are typically required to file IRB checklists.
IRB checklists for universities can be filled out by providing detailed information about the research project, including the purpose of the study, methods used, risks involved, and consent procedures.
The purpose of IRB checklists for universities is to ensure that research projects involving human subjects are conducted ethically and in compliance with regulations to protect the rights and well-being of participants.
IRB checklists for universities typically require information such as study objectives, participant recruitment methods, data collection procedures, and measures to protect confidentiality.
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