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The University of Tulsa Institutional Review Board (TU IRB) INFORMED CONSENT FORM (ICF)GENERAL INSTRUCTIONS * FAQs * ADDITIONAL CONSENT ELEMENTS/SAMPLESPLEASE READ BEFORE COMPLETING THE CONSENT FORM
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Read the informed consent form thoroughly to understand the purpose, risks, benefits, and procedures involved.
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Who needs informed consent form for?

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Informed consent forms are typically required for participants in research studies, clinical trials, medical procedures, and other situations where individuals are asked to voluntarily participate in a study or treatment.

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The informed consent form is used to provide individuals with detailed information about a research study or medical procedure, including the potential risks and benefits, so they can make an informed decision about whether or not to participate.
Researchers, medical professionals, or institutions conducting the research study or medical procedure are required to file an informed consent form for participants.
The informed consent form should be filled out by including all relevant information about the study or procedure, ensuring that participants understand the risks and benefits, and obtaining their signature to indicate their consent.
The purpose of the informed consent form is to protect the rights and well-being of participants by ensuring they have enough information to make an informed decision about whether or not to participate.
The informed consent form must include information about the study or procedure, potential risks and benefits, confidentiality measures, contact information for questions or concerns, and the participant's rights.
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