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ACRP ACRP-CP Exam Syllabus Topics:

ACRP Certified Professional Sample Questions:

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

2. Who takes responsibility for initiating a clinical trial?

A) CRO
B) IRB/IEC
C) Investigator
D) Sponsor

3. Source data/documentation should be:

A) Attributable, legible, correct, original, accurate, and complete.
B) Attributable, legible, correct, original, accurate, and clear.
C) Attributable, legible, contemporaneous, original, accurate, and complete.
D) Attributable, legible, contemporaneous, original, accurate, and clear.

4. Who is responsible for the ongoing safety evaluation of the IP?

A) Regulatory agency
B) IRB/IEC
C) Sponsor
D) PI

5. A clinical trial where participants will be randomized to receive a sequence of two medications has which design configuration?

A) Parallel Group
B) Group sequential
C) Crossover
D) Factorial

Solutions: