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Citiprogram.org Researcher must have completed IRB-approved human research protections training through CITI. AUM IRB Protocol Form 3. 11 AUM Research Protocol Review Form Institutional Review Board for Research Involving Human Subjects Office of Sponsored Programs OSP 114 Administration Bldg 334. Citiprogram.org CITI completion report attached Name Department Faculty Staff Graduate Student Undergraduate Student Role/Responsibility Investigator must have completed IRB-approved human research...
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How to fill out aum irb protocol form

01
Start by downloading the AUM IRB protocol form from the official website.
02
Read the instructions carefully to understand the requirements and guidelines.
03
Provide your personal information in the designated sections, including your name, contact details, and affiliation.
04
Clearly state the purpose and objectives of your research project.
05
Include a detailed methodology section, describing the research design, data collection methods, and analysis techniques.
06
If applicable, explain the potential risks and benefits associated with your study.
07
Provide a list of references and resources that support your research proposal.
08
Ensure that all necessary signatures and approvals are obtained before submitting the form to the AUM IRB office.
09
Double-check your form for any errors or missing information before final submission.

Who needs aum irb protocol form?

01
Researchers planning to conduct studies involving human subjects or sensitive data need an AUM IRB protocol form.
02
Students undertaking research projects as part of their academic curriculum should also fill out the form.
03
Faculty members and staff engaged in research activities under AUM's jurisdiction are required to submit the protocol form.
04
Any individual or organization conducting research with AUM-affiliated participants or resources must complete the form.
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The AUM IRB protocol form is a document used to outline the research plan and ethical considerations for a study involving human subjects.
Researchers conducting studies involving human subjects are required to file an AUM IRB protocol form.
To fill out an AUM IRB protocol form, researchers must provide detailed information about the study design, risks and benefits to participants, and steps taken to ensure ethical conduct.
The purpose of an AUM IRB protocol form is to ensure that research involving human subjects is conducted in an ethical and responsible manner.
Information that must be reported on an AUM IRB protocol form includes study procedures, potential risks to participants, informed consent process, and confidentiality measures.
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