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Rockefeller University Institutional Review Board IRB NUMBER: AAU0112 IRB APPROVAL DATE: 02/04/2018 IRB EXPIRATION DATE: 02/03/2019Clinical Investigation Consent Form The Rockefeller University Hospital
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Step 1: Start by reading the consent form carefully and make sure you understand the contents.
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Step 2: Provide your personal information as requested in the form, such as your name, contact details, and any other required information.
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Step 3: Review the purpose and scope of the consent form to understand what you are giving your consent for.
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Step 4: If there are any sections or statements that you are unsure about, seek clarification from the relevant authority or organization.
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Step 5: Once you are confident and comfortable with the consent form, sign and date it in the designated section.
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Step 6: Make sure to keep a copy of the signed consent form for your own records.
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Step 7: If there are any updates or changes to the consent form in the future, you may be required to provide your consent again.

Who needs userfriendly consent form?

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Userfriendly consent forms are needed by any organization, institution, or individual that collects personal information or seeks consent from individuals for specific purposes.
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This can include businesses, healthcare providers, educational institutions, research organizations, and government agencies, among others.
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By using a userfriendly consent form, these entities can ensure that individuals understand and can provide informed consent for the relevant activities or processes.
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