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ACU IRB # ___Date of Approval __/__/___ Date of Expiration __/__/___Instructions: ALL RED TEXT IS INSTRUCTIONAL. PLEASE DELETE FROM YOUR FINAL DOCUMENT. This template may be used to help you build
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IRB FAQs - Office refers to frequently asked questions concerning the Institutional Review Board (IRB) procedures and policies for offices, particularly how they pertain to research ethics.
Research institutions, investigators, and any personnel involved in studies requiring IRB approval are typically required to understand and adhere to the guidelines set forth in the IRB FAQs - Office.
To fill out the IRB FAQs - Office, one should carefully read the provided questions and answers, ensure that the necessary information is gathered, and submit inquiries or clarifications as necessary.
The purpose of the IRB FAQs - Office is to provide clear guidance and support to those involved in research, ensuring compliance with ethical standards and regulatory requirements.
The information to be reported typically includes research study details, ethical considerations, consent processes, and compliance with IRB regulations.
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