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AUBURN UNIVERSITY INSTITUTIONAL REVIEW BOARD for RESEARCH INVOLVING HUMAN SUBJECTS PROTOCOL REVIEW FORM FULL BOARD or EXPEDITED REVIEWFor assistance, contact: The Office of Research Compliance (ORC)
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How to fill out protocol review form full

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To fill out the protocol review form in full, follow these steps:
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Start by carefully reviewing the form and its instructions to familiarize yourself with the required information.
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Begin by providing your personal details such as name, contact information, and any relevant affiliations.
04
Clearly state the purpose of the protocol and provide a brief summary of the research study.
05
Include a detailed description of the study design, methodology, and any experimental procedures involved.
06
Specify the target population and any inclusion or exclusion criteria for participants.
07
Clearly outline the potential risks and benefits associated with the study and provide any measures taken to ensure participant safety.
08
Document any informed consent procedures implemented and detail how confidentiality and privacy will be maintained.
09
Include information about the resources and funding required for the study.
10
Provide a timeline for the study's execution, including anticipated start and end dates.
11
If applicable, include any references or previous studies that support the need for the current research.
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Review the completed form for accuracy and make any necessary revisions before submitting.
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Submit the filled-out protocol review form through the designated channels as instructed.

Who needs protocol review form full?

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Protocol review form full is typically needed by researchers, scientists, or academic professionals who are planning to conduct a research study or experiment that requires ethical approval.
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Universities, research institutions, and ethical review boards often require researchers to submit a filled-out protocol review form for assessment and approval.
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Individuals involved in medical or clinical research, social science investigations, or any study involving human subjects may need to complete this form.
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The form helps to ensure that research activities follow ethical guidelines, protect the rights of participants, and minimize any potential risks.

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The protocol review form full is a comprehensive document used to evaluate and ensure that a research project adheres to ethical standards, regulatory requirements, and organizational guidelines.
Researchers, investigators, or institutions conducting studies involving human subjects or animals are typically required to file the protocol review form full.
To fill out the protocol review form full, one should gather all relevant project information, complete each section of the form accurately, provide detailed descriptions of the study design, methodology, and any potential risks, and submit the form to the appropriate review board or committee.
The purpose of the protocol review form full is to ensure that research proposals are thoroughly evaluated for ethical considerations, participant safety, scientific validity, and compliance with federal and institutional regulations.
Key information to report includes the study title, principal investigator details, a summary of the research objectives, study design, participant recruitment methods, informed consent procedures, and risk assessment.
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