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ACRP Certified Professional Sample Questions:

1. Which of the following should be reviewed and evaluated by qualified experts to assess implications for the safety of the trial subjects?

A) PI roles and responsibilities
B) Emerging animal toxicological and clinical data
C) Sample collection storage, disposal, and shipment requirements
D) Project feasibility considerations

2. At a close-out visit, which document should be retained only at the site?

A) Treatment allocation
B) Subject identification code list
C) Final trial close-out monitoring report
D) IP accountability

3. Who should vote during the IRB/IEC review and discussion process?

A) All IRB/IEC members and non-member experts
B) All members who were involved in the review and discussion
C) All IRB/IEC members
D) All members who were involved in the review and discussion and non-member experts

4. Which statement does NOT represent a study monitor's responsibilities?

A) Report serious adverse events to the IRB/IEC.
B) Verify that the PI has adequate qualifications and resources to conduct the study.
C) Check the accuracy and completeness of case report forms with source documents.
D) Provide communication between the sponsor and the PI.

5. In preparation for an upcoming site audit, whose responsibility is it to ensure study-related functions were conducted by qualified personnel?

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

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