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HREB Version April 2023Instructions for Informed Consent Form Development The informed consent form (ICF) is one component of the informed consent process. Further guidance may be found in the HREB
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How to fill out the informed consent form

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Make sure to read the informed consent form thoroughly before filling it out.
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Provide all the required information honestly and accurately.
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Sign and date the form to indicate your consent.
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Keep a copy of the filled out form for your records.

Who needs the informed consent form?

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Anyone who is participating in a research study, medical procedure, or any activity that requires voluntary consent should fill out an informed consent form.
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The informed consent form is a document that explains the study or procedure to the participant.
Researchers or medical professionals conducting the study are required to file the informed consent form.
Fill out the form with detailed information about the study, risks, benefits, and participant rights.
The purpose of the informed consent form is to ensure that participants understand the study and give their voluntary consent to participate.
Information on the study purpose, procedures, risks, benefits, and participant rights must be reported on the informed consent form.
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