The follow-up visit is significant because any trends or discrepancies in the participant's lab results can be detected and the PI will be made aware of the issue.
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Q7: In clinical research, the purpose is to
Q8: Verbal consents between participants and the researcher
Q9: To be eligible to participate in a
Q10: Research participants must be protected and well-informed
Q11: All clinical research studies will use a
Q13: Participants are typically randomized to their study
Q14: Once the study medication or device is
Q15: The term adverse events and significant adverse
Q16: When conducting clinical research, the two most
Q17: Which is a role of the study
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