ACRP ACRP Certified Professional ACRP-CP

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ACRP Certified Professional Sample Questions:

1. In preparation for an upcoming site audit, whose responsibility is it to ensure study-related functions were conducted by qualified personnel?

A) Sponsor
B) CRA
C) Investigator
D) CRC

2. Who is responsible for securing agreement from all involved parties to ensure direct access of all trial-related source documents?

A) Sponsor
B) CRO
C) Investigator
D) CRC

3. The process of ensuring and documenting that an electronic data processing system conforms to the sponsor's established requirements for completeness, accuracy, reliability, and consistent intended performance is called:

A) Validation
B) Programming
C) Quality Assurance
D) Quality Control

4. A study protocol must contain which of the following elements?

A) Data management plan
B) Description of statistical methods
C) Participant reimbursement details
D) Chemical structure of the IP

5. A deferred consent can take place in which of the following situations?

A) Only when the PI approves such a consent process, regardless of the emergency situation described in the protocol.
B) In an emergency situation only, when this process is described in the protocol and has received permission from the ethics committee.
C) Only when the PI approves such a consent process immediately prior to patient enrollment, regardless of the situation being classed as emergency.
D) In an emergency situation only, even when this process is not described in the protocol, but the sponsor approves the consent process.

Solutions: