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UNIVERSITY OF PENNSYLVANIA HEALTH SYSTEM Gilead Sciences, Inc GSUS2360102, Amendment 2, 19JAN2012 A Phase 3, Randomized, DoubleClick Study to Evaluate the Safety and Efficacy of Elvitegravir// Bisoprolol

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What is irb approved bfromb 28-mar-b2013b?

irb approved bfromb 28-mar-b2013b refers to a document or form that has been approved by the Institutional Review Board (IRB) on March 28, 2013. It is used to report certain information or comply with specific regulations.

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The purpose of irb approved bfromb 28-mar-b2013b is to ensure that research involving human subjects is conducted ethically and in compliance with applicable regulations and guidelines. It serves as a tool to report and document the necessary information for IRB review and approval.

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The specific information that must be reported on the irb approved bfromb 28-mar-b2013b may vary depending on the requirements of the IRB and the nature of the research. However, commonly reported information includes details about the study purpose, methodology, participant characteristics, data collection procedures, informed consent process, privacy and confidentiality measures, and potential risks or benefits.

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