Once the study medication or device is approved, the FDA does not require continued data collection.
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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
Q13: Participants are typically randomized to their study
Q15: The term adverse events and significant adverse
Q16: When conducting clinical research, the two most
Q17: Which is a role of the study
Q18: The clinical research associate is responsible for:
A)
Q19: Per ICH E6 Guidelines and FDA Code
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