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ACRP Certified Professional Sample Questions:

1. Who is responsible for the ongoing safety evaluation of the IP?

A) Sponsor
B) IRB/IEC
C) PI
D) Regulatory agency

2. When determining whether a protocol deviation (PD) is reportable to the IRB/IEC, the PI should take into consideration whether the:

A) Sponsor approved the PD.
B) PD affected participant safety.
C) Participant verbally agreed to the PD.
D) PD affected participant recruitment.

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) Contemporaneous
D) Original

4. Who ensures information regarding payments to subjects is documented in a written consent form?

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

5. The coding system for a double-blind clinical trial is accessible by the:

A) Sponsor
B) IRB/IEC
C) PI
D) Regulatory authority

Solutions: