ACRP ACRP-CP : ACRP Certified Professional Exam

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ACRP Certified Professional Sample Questions:

1. The investigator/institution should permit:

A) Monitoring and auditing by the sponsor, and inspection by the appropriate regulatory authority(ies).
B) Monitoring and auditing by the appropriate regulatory authority(ies), and inspection by the sponsor.
C) Monitoring and inspection by the appropriate regulatory authority(ies), and auditing by the sponsor.
D) Monitoring and inspection by the sponsor, and auditing by the appropriate regulatory authority(ies).

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

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

3. IP is dispensed to all subjects who:

A) Are eligible to receive it in the trial.
B) Need IP for their medical condition.
C) Screened for the trial.
D) Consented for the trial.

4. A quality assurance audit of the EDC system SOP revealed a deficiency. Which of the following is the MOST likely reason?

A) The frequency of data backup was not defined.
B) The number of unique eCRF templates was not specified.
C) The list of comparable technology solutions was not included.
D) The number of users with access was not defined.

5. Which document confirms the PI's agreement to permit auditing at the study site?

A) IB
B) Delegation Log
C) Protocol
D) ICF

Solutions: