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The Informed Consent Document should not be used as a data collection tool. For example, collection of address, e-mail, screening information, phone numbers, SSN, hospital number, appointment scheduling, or other study data must not be collected on this document. Such information should be collected on a separate document. The use, storage and disposal (as applicable) of this information must be described in the HawkIRB application for review and approval by the IRB.