ACRP ACRP-CP : ACRP Certified Professional Exam

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ACRP ACRP-CP Exam Syllabus Topics:

ACRP Certified Professional Sample Questions:

1. Who is responsible for securing agreement from all involved parties to ensure direct access of all trial-related source documents?

A) Investigator
B) CRO
C) CRC
D) Sponsor

2. What is a systematic and independent examination of trial-related activities and documents todetermine whether the evaluated trial-related activities were conducted and the data were recorded, analyzed, and accurately reported according to the protocol, sponsors, SOPs, GCP, and the applicable regulatory requirements?

A) Audit
B) Site qualification
C) Inspection
D) Routine monitoring

3. The process of ensuring and documenting that an electronic data processing system conforms to the sponsor's established requirements for completeness, accuracy, reliability, and consistent intended performance is called:

A) Quality Assurance
B) Quality Control
C) Validation
D) Programming

4. 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?

A) Use a central IRB/IEC.
B) Decline the study.
C) Recruit for the study without use of social media.
D) Rely on the sponsor to notify the IRB/IEC.

5. A sponsor wants a new clinical trial to be reviewed at regular intervals for progress, safety, and endpoint evaluation, and make recommendations to continue, modify, or stop the trial. How should they proceed?

A) Develop a monitoring plan
B) Conduct routine investigators' meetings
C) Draft a CAPA plan
D) Establish a DSMB/IDMC

Solutions: