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

2. A clinical trial where participants will be randomized to receive a sequence of two medications has which design configuration?

A) Parallel Group
B) Factorial
C) Group sequential
D) Crossover

3. A PI is reviewing the CRF for a recent subject visit and notices the participant's heart rate and temperature are not recorded. Which of the following study documentation practices was neglected?

A) Original
B) Complete
C) Attributable
D) Contemporaneous

4. Which of the following documents is maintained by a PI to ensure compliance with sponsor requirements?

A) Training records of site personnel on study protocol, and their study-related duties and functions.
B) Regulatory submission of protocol and accompanying documents to relevant regulatory authority.
C) A monitoring plan that is tailored to the specific human subject protection and data integrity risks of the trial.
D) A monitoring report that identifies deviation from the approved protocol.

5. Which strategy is used to safeguard subject privacy?

A) Conduct subject-related conversations in controlled environments.
B) Store source documentation in the CRC's office.
C) Utilize subject initials on correspondence.
D) Email updated enrollment logs to the CRA.

Solutions: