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For more information on assent please refer to the HRPP SOP Manual on the g drive or contact the IRB Office. ClinicalTrials. gov For applicable clinical trials initiated on or after March 7 2012 the following language will now be required by the FDA. For more information regarding emancipated minors please contact the HRPP Director or the IRB Manager. An assent form and process is still encouraged in such studies for children who are capable of providing assent since the goal of IRB Office...
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