CH Guidelines and FDA support the practice of "prequalifying" patients for a research study.
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Q1: The overall goal of clinical research is
Q2: Co-investigators retain the sole responsibility for the
Q3: The PI overseas any adverse events in
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
Q10: Research participants must be protected and well-informed
Q11: All clinical research studies will use a
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