In clinical research, the purpose is to translate laboratory research into applied clinical interventions.
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Q2: Co-investigators retain the sole responsibility for the
Q3: The PI overseas any adverse events in
Q4: CH Guidelines and FDA support the practice
Q5: The number of and severity of adverse
Q6: During Phase IV of clinical studies, the
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
Q12: The follow-up visit is significant because any
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