최신 ACRP-CP 무료덤프 - ACRP Certified Professional
A new device trial is being considered. Before committing to participate in the trial, what is the MOST important item the PI needs to evaluate?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
Who on the local site research study team is accountable for the unblinding documentation of IP?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
During a monitoring visit, a CRA notices that a piece of equipment required for the study needs to be serviced. Who is responsible for addressing this problem?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
A study sponsor approaches a facility about participating in their research study. The study sponsor requires use of social media as its sole method of recruitment. The site knows their institutional IRB/IEC does not approve of social media recruiting. How should the site respond?
정답: C
설명: (DumpTOP 회원만 볼 수 있음)
An audit was recently completed and identified non-compliance that could potentially affect the reliability of study results. Who should perform a root cause analysis and implement appropriatecorrective and preventive actions?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
The PI should ensure that source data is:
정답: A
설명: (DumpTOP 회원만 볼 수 있음)
Who takes responsibility for initiating a clinical trial?
정답: B
설명: (DumpTOP 회원만 볼 수 있음)
The inclusion and exclusion criteria are in place so all subjects are:
정답: C
설명: (DumpTOP 회원만 볼 수 있음)
Which statement does NOT represent a study monitor's responsibilities?
정답: B
설명: (DumpTOP 회원만 볼 수 있음)
Who is responsible for outlining written procedures in a study to assure that changes or corrections in CRFs are documented, are necessary, and are endorsed by the investigator?
정답: A
설명: (DumpTOP 회원만 볼 수 있음)