SOCRA CCRP EXAM
ACTUAL EXAM 200
QUESTIONS AND
CORRECT DETAILED
ANSWERS WITH
RATIONALES
|AGRADE|2024
ICF✔✔✔ANSWER➖An informed consent form (ICF) is
used to ensure everyone involved in clinical research is a
willing participant, with full knowledge of the potential
risks and benefits to the extent that this is possible.
ICH✔✔✔ANSWER➖This International Conference on
Harmonization (ICH) document makes recommendations
on information that should be included in a core clinical
study report of an individual study of any therapeutic,
prophylactic, or diagnostic agent conducted in human
subjects.
IRB✔✔✔ANSWER➖Institutional Review Board (IRB)?
Under FDA regulations, an IRB is an appropriately
constituted group that has been formally designated to
review and monitor biomedical research involving human
subjects.
IR
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