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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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Provide your consent by signing and dating the form at the appropriate section.
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Who needs optional-study-consent-template-april-2023-1?
01
Individuals who are participating in an optional study that requires providing consent.
02
Researchers or institutions conducting studies that mandate obtaining consent from participants.
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What is optional-study-consent-template-april-1?
The optional-study-consent-template-april-1 is a form used to obtain consent from participants in optional research studies.
Who is required to file optional-study-consent-template-april-1?
Researchers conducting optional research studies are required to file the optional-study-consent-template-april-1 form.
How to fill out optional-study-consent-template-april-1?
The optional-study-consent-template-april-1 form should be filled out by providing information about the study, risks and benefits, voluntary participation, confidentiality, and contact information.
What is the purpose of optional-study-consent-template-april-1?
The purpose of the optional-study-consent-template-april-1 is to ensure that participants in optional research studies are fully informed and give voluntary consent to participate.
What information must be reported on optional-study-consent-template-april-1?
The optional-study-consent-template-april-1 should include details about the study, risks and benefits, confidentiality measures, contact information, and the voluntary nature of participation.
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