ACRP ACRP-CP : ACRP Certified Professional Exam

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ACRP Certified Professional Sample Questions:

1. While consenting a potential subject, a coordinator discovered the subject could not read. Under what conditions can this potential subject be enrolled?

A) Locate a translator and have them work with the person.
B) Have the Principal Investigator consent the person.
C) There are no circumstances under which this person can be enrolled.
D) Get an impartial witness involved in consenting this person.

2. Who is responsible to ensure training for key staff members unable to attend the site initiation visit?

A) Monitor
B) Sponsor
C) Coordinator
D) Investigator

3. An interim analysis is conducted during a clinical trial. To review the results, the sponsor assigns:

A) Investigators participating in the trial.
B) Regulatory authority expert advisors.
C) Independent qualified individuals.
D) Executive board members.

4. The composition of an IDMC/DSMB should include which one of the following?

A) A sponsor representative who is knowledgeable about the study's unblinded information
B) A lead PI for the study
C) A clinical scientist who is knowledgeable in the appropriate discipline
D) A member from the IRB/IEC

5. A potential subject is interested in a new clinical trial and would like to learn more about the risks and benefits of participation. Where can they find this information?

A) ICF
B) Package insert
C) Protocol
D) IB

Solutions: