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IRB PROTOCOL # 073619FBPage 1 of 10ADULT CONSENT CLINICAL BIOMEDICALTitle of this Research StudyInvitation and Summary You are invited to be in this research study. Taking part in this research is
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irb protocol 0736-19-fb is a specific protocol number assigned to a research study by an Institutional Review Board.
The principal investigator of the research study is required to file irb protocol 0736-19-fb.
To fill out irb protocol 0736-19-fb, the principal investigator must provide detailed information about the research study, including its purpose, methodology, risks, and benefits.
The purpose of irb protocol 0736-19-fb is to ensure the protection of human subjects participating in research studies.
Information that must be reported on irb protocol 0736-19-fb includes details about the study design, informed consent process, risk assessment, and procedures for monitoring subject safety.
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