Research participants must be protected and well-informed of their study status at all times during a clinical study.
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Q5: The number of and severity of adverse
Q6: During Phase IV of clinical studies, the
Q7: In clinical research, the purpose is to
Q8: Verbal consents between participants and the researcher
Q9: To be eligible to participate in a
Q11: All clinical research studies will use a
Q12: The follow-up visit is significant because any
Q13: Participants are typically randomized to their study
Q14: Once the study medication or device is
Q15: The term adverse events and significant adverse
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