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ACRP ACRP-CP Exam Syllabus Topics:

ACRP Certified Professional Sample Questions:

1. Which of the following reports should be retained in participant charts?

A) Lab reports
B) Safety reports
C) IRB/IEC progress reports
D) DSMB/IDMC reports

2. Which of the following activities would be undertaken by the sponsor to BEST ensure overall quality of the study data?

A) Conduct annual reviews of the protocol and accompanying study documents.
B) Ensure there is an accompanying written record that describes the consent process.
C) Develop a plan that describes the monitoring approach for a clinical study.
D) Ensure submission of a data management plan to the regulatory authorities.

3. When assessing the monitoring needs for a study, sponsors should:

A) Ensure monitoring visits are conducted at periodic intervals with a minimum of monthly monitoring visits.
B) Use central monitoring instead of conducting physical monitoring visits at sites.
C) Permit PIs to select a monitor for their site as long as they are independent of the PI.
D) Ensure monitors have the scientific and/or clinical knowledge needed to monitor the trial adequately.

4. The primary purpose for IRB/IEC approval of posters, fliers, social media posts, and promotional items is to:

A) Assure the ads do not impinge on confidentiality agreements.
B) Safeguard the rights, safety, and well-being of all potential subjects.
C) Review the content for ethically or morally sensitive issues.
D) Confirm subjects receive the appropriate reimbursement.

5. In addition to members who collectively have the qualifications and experience to review and evaluate the science, medical aspects, and ethics of the proposed trial, it is recommended that the IRB/IEC should include:

A) One member of the site's QA group.
B) One member whose primary area of interest is in the same scientific area.
C) One member who is independent of the institution/trial site.
D) A total of five members.

Solutions: