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(Hawk ACT) Applicable Clinical Trial Checklist Study Title (required): This form is optional. Investigators using drugs, devices, or biologics in research may complete this form to:1) Provide direct

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How to fill out hawkirb - human subjects

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Step 1: Obtain the necessary forms and guidelines for filling out the HawkIRB - Human Subjects application.

02

Step 2: Fill out the application form accurately and completely.

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Step 3: Provide detailed information about the research study, including the purpose, methods, and expected outcomes.

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Step 4: Include information about the potential risks and benefits of participation for human subjects.

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Step 5: Attach any supporting documents required, such as consent forms, recruitment materials, or survey instruments.

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Step 6: Review the completed application for any errors or missing information.

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Step 7: Submit the filled-out HawkIRB - Human Subjects application to the appropriate review board or committee for evaluation.

Who needs hawkirb - human subjects?

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Researchers or individuals conducting research studies involving human subjects need to fill out HawkIRB - Human Subjects application.

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Institutions, organizations, or agencies that require ethical approval for human subjects research also need to use HawkIRB.

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What is hawkirb - human subjects?

HawkIRB - Human Subjects is an online system for the submission, review, and management of human subjects research conducted by University of Iowa researchers.

Who is required to file hawkirb - human subjects?

University of Iowa researchers conducting human subjects research are required to file through HawkIRB - Human Subjects.

How to fill out hawkirb - human subjects?

Researchers can fill out HawkIRB - Human Subjects by logging into the online system, completing the required forms, and submitting all necessary documentation.

What is the purpose of hawkirb - human subjects?

The purpose of HawkIRB - Human Subjects is to ensure that research involving human subjects is conducted ethically and in compliance with regulatory requirements.

What information must be reported on hawkirb - human subjects?

Researchers must report details about the study design, risks to participants, informed consent procedures, and data management plans on HawkIRB - Human Subjects.

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