最新のACRP-CP問題集で試験を準備する

ACRP ACRP-CP 試験概要:

ACRP ACRP-CP 試験シラバストピック:

ACRP Certified Professional 認定 ACRP-CP 試験問題：

1. An investigator in a multicenter trial reports multiple occurrences of an SAE to the sponsor. Who is responsible for reporting the SAEs to the remaining sites' IRB/IECs?

A) Investigator at each site
B) Regulatory authority
C) Original reporting investigator
D) Study sponsor

2. A study is using an EDC system. After the data is entered into EDC, who is the next to review and conduct SDV of this data?

A) Monitor
B) Data Manager
C) QA Department
D) Sponsor

3. A clinical trial is conducted to measure the effectiveness of music therapy to reduce anxiety in intensive care unit patients. Patients are randomly assigned to receive headphones with music of their choice or headphones with white noise. The group receiving the white noise headphones is considered which type of control group?

A) No treatment
B) Placebo
C) Alternate dose
D) Active control

4. An impartial witness should be present during the entire informed consent discussion when:

A) A parent/guardian is consenting for a minor subject.
B) A legally acceptable representative is unable to read.
C) A subject has been determined to be vulnerable.
D) An interpreter is translating the consent form for a subject.

5. The sponsor should supply a PI with the IP after:

A) Approval of protocol by the PI.
B) Submission of documents to IRB/IEC and regulatory authority for review.
C) Approval/favorable opinion from IRB/IEC and regulatory authority.
D) Approval of protocol by the sponsor.

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