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Appendix D: Access to Data and Aggregate Reporting Research Data Request Form for Use of Aggregate Data: Eligibility Criteria for Participating Centers (The RSS will not be held to below criteria)
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Researchers who are conducting studies involving human subjects.
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Institutional Review Board (IRB) members who review and approve research protocols.
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Healthcare professionals involved in clinical trials or research studies.
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IRB frequently asked questions are commonly asked questions related to Institutional Review Board processes and regulations.
Researchers, institutions, and organizations conducting research involving human subjects are required to file IRB frequently asked questions.
IRB frequently asked questions can be filled out online through the designated platform provided by the Institutional Review Board.
The purpose of IRB frequently asked questions is to ensure that research involving human subjects is conducted ethically and within regulatory guidelines.
IRB frequently asked questions may require information such as study protocols, risks and benefits to participants, informed consent processes, and safeguards for confidentiality.
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