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Rockefeller University Institutional Review Board IRB NUMBER: AAU-0112 IRB APPROVAL DATE: 03/27/2013 IRB EXPIRATION DATE: 03/26/2014 Clinical Investigation Consent Form The Rockefeller University
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Start by reading the consent form thoroughly to understand its purpose and what information you are consenting to.
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The user friendly consent form is a document that is designed to be easy for users to understand and consent to the terms and conditions of a service or product.
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The purpose of a user friendly consent form is to ensure that individuals are informed about the terms and conditions of a service or product, and to obtain their consent in a clear and easily understandable manner.
The specific information that must be reported on a user friendly consent form may vary depending on the purpose and requirements of the form. Commonly reported information includes personal details, the nature of the service or product, and any associated terms and conditions.
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