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FHCDA CONSENT FORM 2

FHCDA CONSENT FORM 2

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foreign [Music] Clips my name is Harsha rajasimha and today I will be talking to you about informed consent for clinical trials or general research studies as you may know a research study involving human participants must be approved by an Institutional review board or IRB and IRB is a diverse team of individuals with a shared responsibility to protect the rights and well-being of humans participating in research once the IRB approves the study the researcher can start recruiting eligible participants as an eligible participant you can only join the study if you provide consent consent is voluntary and must be informed through a process in which the researcher clearly communicates that you are participating in a study the nature and goal of the study clarifying what your role will be what will happen during the study and how much time it will take the risks are discomforts of participating the potential benefits of the study your rights as a participant including that your participati

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