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UNIVERSITY OF AKRON GUIDELINES FOR CLASSROOMBASED PROTOCOLS UTILIZING HUMAN SUBJECTS The Institutional Review Board (IRB) for the Protection of Human Subjects recognizes that many student research

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How to fill out u of akron irb

01

Start by logging into the U of Akron IRB online system using your university credentials.

02

Select the type of application you want to submit (ex: new study, modification, renewal, etc)

03

Fill out all required sections of the application form, including study information, participant information, risks and benefits, etc.

04

Upload any additional documents required for the application (ex: consent forms, questionnaires, recruitment materials)

05

Review your application for any errors or missing information before submitting it for review.

06

Submit your application and wait for approval or feedback from the IRB committee.

Who needs u of akron irb?

01

Researchers conducting studies involving human participants at the University of Akron need to fill out the U of Akron IRB.

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What is u of akron irb?

The University of Akron's Institutional Review Board (IRB) is a committee responsible for reviewing and approving research protocols involving human subjects to ensure their ethical conduct.

Who is required to file u of akron irb?

Researchers and faculty members conducting research involving human subjects at the University of Akron are required to file an IRB application.

How to fill out u of akron irb?

To fill out the University of Akron IRB application, researchers must provide detailed information about their research protocol, including the study design, procedures, risks, and benefits.

What is the purpose of u of akron irb?

The purpose of the University of Akron IRB is to protect the rights and welfare of human subjects participating in research studies conducted at the university.

What information must be reported on u of akron irb?

Researchers must report detailed information about their research protocol, including the study design, procedures, risks, benefits, and informed consent process.

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