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ACRP ACRP-CP Exam Syllabus Topics:

ACRP Certified Professional Sample Questions:

Question 1

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

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

Question 2

All of the following are steps to assure an effective risk management approach while conducting a clinical study EXCEPT:

A. Identifying potential study risks.
B. Documenting all possible risk scenarios.
C. Controlling risk by setting thresholds of risk acceptability.
D. Assessing risk based on study impact.

Question 3

IP is dispensed to all subjects who:

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

Question 4

In order to conduct open-label, parallel group clinical trials according to sound scientific principles, which of the following design elements should be included?

A. Blinding
B. Placebo-controlled
C. Randomization
D. Privacy controls

Question 5

The inclusion and exclusion criteria are in place so all subjects are:

A. Ethically vulnerable and patients with the disease under study.
B. Healthy and willing to complete the clinical trial.
C. Medically appropriate and protected from ethical vulnerability.
D. Patients with the disease under study and will not have any adverse events.

Solutions: