최신 ACRP-CP 무료덤프 - ACRP Certified Professional
Which entity has ultimate responsibility over the conduct of the multi-center clinical trial?
정답: B
설명: (DumpTOP 회원만 볼 수 있음)
What would a sponsor use to implement and maintain quality in a study?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
After the completion or termination of a clinical trial, who should store the enrollment log?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
The PI did not record the relationship to IP in the medical chart when assessing an adverse event. The CRC noticed the omission and brought it to the PI's attention. How should this be addressed?
정답: D
설명: (DumpTOP 회원만 볼 수 있음)
Who must be blinded in a double-blind study in order to prevent bias?
정답: C
설명: (DumpTOP 회원만 볼 수 있음)
In an investigator-initiated study, who is responsible for implementing appropriate corrective and preventive actions when significant non-compliance is discovered?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
In preparation for an upcoming site audit, whose responsibility is it to ensure study-related functions were conducted by qualified personnel?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
After enrolling and treating a few subjects on an investigator-initiated trial, the PI would like to include a subject diary for each trial subject to capture their activities and experiences on the trial regimen. After the PI has generated a diary, what should the PI do next?
정답: C
설명: (DumpTOP 회원만 볼 수 있음)
An impartial witness should be present during the entire informed consent discussion when:
정답: B
설명: (DumpTOP 회원만 볼 수 있음)
A root cause analysis should be:
정답: B
설명: (DumpTOP 회원만 볼 수 있음)