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UCI IRB: Biomed Consent February 2016UNIVERSITY OF CALIFORNIA, IRVINE CONSENT TO ACT AS A HUMAN RESEARCH SUBJECT A phase IIa, randomized, doubleblind, placebocontrolled study of the safety and efficacy
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The purpose is to ensure transparency and compliance with legal requirements when collecting and reporting data for specific uses.
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Information that must be reported includes personal data, consent documentation, and any relevant metrics or identifiers as mandated by law.
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