ACRP ACRP-CP - ACRP Certified Professional Exam

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ACRP ACRP-CP Exam Syllabus Topics:

ACRP Certified Professional Sample Questions:

1. The process of ensuring and documenting that an electronic data processing system conforms to the sponsor's established requirements for completeness, accuracy, reliability, and consistent intended performance is called:

A) Quality Control
B) Quality Assurance
C) Programming
D) Validation

2. Centralized monitoring can:

A) Indicate the need to send monitors to perform onsite visits.
B) Enable appropriate stratification of subject enrollment.
C) Confirm why sites are deviating from the protocol.
D) Identify IP accountability and storage issues.

3. A potential subject is interested in a new clinical trial and would like to learn more about the risks and benefits of participation. Where can they find this information?

A) ICF
B) Package insert
C) IB
D) Protocol

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

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

5. A protocol amendment is needed to collect additional data from a participant's medical record. When can the research team begin collecting the additional data?

A) As soon as the protocol amendment is submitted to the IRB/IEC
B) After the original planned data collection is completed
C) After the protocol amendment is approved by the IRB/IEC
D) When the need for the additional data is discovered

Solutions: