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ACRP Certified Professional Sample Questions:

1. Who determines the age of assent for pediatric studies?

A) IRB/IEC
B) PI
C) Parent
D) Sponsor

2. In order to conduct open-label, parallel group clinical trials according to sound scientific principles, which of the following design elements should be included?

A) Blinding
B) Privacy controls
C) Randomization
D) Placebo-controlled

3. The primary purpose for IRB/IEC approval of posters, fliers, social media posts, and promotional items is to:

A) Review the content for ethically or morally sensitive issues.
B) Assure the ads do not impinge on confidentiality agreements.
C) Confirm subjects receive the appropriate reimbursement.
D) Safeguard the rights, safety, and well-being of all potential subjects.

4. Which of the following reports should be retained in participant charts?

A) IRB/IEC progress reports
B) DSMB/IDMC reports
C) Lab reports
D) Safety reports

5. 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?

A) The PI should notify the monitor.
B) The CRC should amend the medical chart.
C) The CRC should write a note to file.
D) The PI should amend the medical chart.

Solutions: