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ACRP Certified Professional Sample Questions:

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

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

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

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) Complete
B) Attributable
C) Original
D) Contemporaneous

4. A sponsor wants to transfer duties to a CRO. Which of the following statements is the MOST correct?

A) Regulatory authorities must be notified promptly of the transfer of any duties to a CRO.
B) The IRB/IEC must approve the transfer of duties to a CRO.
C) All duties transferred to a CRO should be specified in writing.
D) Any trial-related duties can be documented as transferred by verbal agreement.

5. An impartial witness should be present during the entire informed consent discussion when:

A) A subject has been determined to be vulnerable.
B) An interpreter is translating the consent form for a subject.
C) A legally acceptable representative is unable to read.
D) A parent/guardian is consenting for a minor subject.

Solutions: