ACRP ACRP-CP : ACRP Certified Professional Exam

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ACRP ACRP-CP Exam Syllabus Topics:

ACRP Certified Professional Sample Questions:

Question 1

After enrolling and treating a few subjects on an investigator-initiated trial, the PI would like to include a subject diary for each trial subject to capture their activities and experiences on the trial regimen. After the PI has generated a diary, what should the PI do next?

A. Submit the diary to the IRB/IEC for approval.
B. No approval is necessary: give the diary to each subject.
C. Submit the diary to the sponsor for approval.
D. Submit the diary to the regulatory authority for approval.

Question 2

The PI may assign responsibility for IP accountability to the pharmacist provided they are:

A. Approved by the IRB/IEC.
B. An employee of the institution.
C. Under the supervision of the PI.
D. Licensed to practice medicine.

Question 3

Confidentiality and privacy rules for protection of human subjects at research sites are determined by the:

A. PI
B. Applicable regulatory authorities
C. Sponsor
D. Applicable site SOPs

Question 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. Any trial-related duties can be documented as transferred by verbal agreement.
C. The IRB/IEC must approve the transfer of duties to a CRO.
D. All duties transferred to a CRO should be specified in writing.

Question 5

Which strategy is used to safeguard subject privacy?

A. Store source documentation in the CRC's office.
B. Conduct subject-related conversations in controlled environments.
C. Utilize subject initials on correspondence.
D. Email updated enrollment logs to the CRA.

Solutions: