The protection of rights, safety, and well-being of human subjects is the primary responsibility of the
A) protocol document.
B) primary investigator.
C) Institutional Review Board.
D) monitor.
Correct Answer:
Verified
Q7: Original medical records used as documentation in
Q8: Researchers and sponsors must follow privacy protection
Q9: A document that describes the objective(s), design,
Q10: What are the two categories of clinical
Q11: Which term refers to the entity that
Q13: In the U.S., clinical trials must be
Q14: Which acronym is used to aid in
Q15: All of the following must be included
Q16: Which term is defined as a process
Q17: The Food and Drug Administration governs clinical
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