ACRP-CP최고품질덤프문제최신버전인증덤프

ACRP ACRP-CP인증덤프가 KoreaDumps전문가들의 끈임 없는 노력 하에 최고의 버전으로 출시되었습니다. 여러분의 꿈을 이루어드리려고 말이죠. IT업계에서 자기만의 자리를 잡고 싶다면ACRP ACRP-CP인증시험이 아주 좋은 자격증입니다. 만약ACRP ACRP-CP인증시험 자격증이 있다면 일에서도 많은 변화가 있을 것입니다, 연봉상승은 물론, 자기자신만의 공간도 넓어집니다.

KoreaDumps에서 제공해드리는 IT인증시험대비 덤프를 사용해보신적이 있으신지요? 만약에 다른 과목을 사용해보신 분이라면 ACRP ACRP-CP덤프도 바로 구매할것입니다. 첫번째 구매에서 패스하셨다면 덤프에 신뢰가 있을것이고 불합격받으셨다하더라도 바로 환불해드리는 약속을 지켜드렸기때문입니다. 처음으로 저희 사이트에 오신 분이라면ACRP ACRP-CP덤프로 첫구매에 도전해보지 않으실래요? 저희 덤프로 쉬운 자격증 취득이 가능할것입니다.

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최신 ACRP Certified Professional ACRP-CP 무료샘플문제 (Q69-Q74):

질문 # 69
In preparation for an upcoming site audit, whose responsibility is it to ensure study-related functions were conducted by qualified personnel?

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

정답：B

설명：
The Principal Investigator (PI) holds ultimate responsibility for ensuring that all study-related functions are conducted by qualified and trained personnel. The PI must verify that staff have the necessary qualifications and training to perform their assigned tasks as outlined in the protocol. This responsibility is crucial for maintaining compliance with GCP and ensuring data integrity.
According to GCP guidelines, the PI must ensure that all staff assisting with the trial are adequately trained and qualified for their roles.
"The investigator is responsible for ensuring that all persons assisting with the trial are qualified by education, training, and experience to perform their respective tasks." Objectives:
* Maintain compliance with GCP requirements.
* Ensure qualified personnel conduct study tasks.

질문 # 70
The primary purpose for IRB/IEC approval of posters, fliers, social media posts, and promotional items is to:

A. Review the content for ethically or morally sensitive issues.
B. Safeguard the rights, safety, and well-being of all potential subjects.
C. Assure the ads do not impinge on confidentiality agreements.
D. Confirm subjects receive the appropriate reimbursement.

정답：B

설명：
The IRB/IEC's primary responsibility when reviewing recruitment materials such as posters, fliers, social media posts, and promotional items is to ensure that these materials safeguard the rights, safety, and well- being of potential participants. This includes ensuring that the information is presented ethically, clearly, and without coercion, maintaining compliance with ethical guidelines.
GCP guidelines require that any materials used for recruitment be reviewed to ensure they do not mislead participants and that they respect their rights and well-being.
"IRB/IEC review of recruitment materials ensures that they protect participants' rights and well-being and that the content is ethically appropriate." Objectives:
* Maintain ethical standards in recruitment.
* Protect potential participants from misleading or coercive information.

질문 # 71
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. Package insert
B. ICF
C. IB
D. Protocol

정답：B

설명：
The Informed Consent Form (ICF) contains comprehensive information about the potential risks and benefits of participation in a clinical trial. It is a legally required document that ensures that subjects make an informed decision before enrollment.
The answer is consistent with GCP guidelines which mandate that the ICF clearly outlines the risks and benefits of participation to protect participant rights.
"The ICF should include a clear explanation of potential risks and benefits to ensure informed decision- making by the participant." Objectives:
* Ensure informed decision-making by potential subjects.
* Provide transparent risk-benefit information.

질문 # 72
The PI should ensure that source data is:

A. Kept on site for a minimum of 2 years.
B. On worksheets that are provided by the sponsor.
C. Printed directly from the EMR.
D. Accurately reflected in the eCRFs.

정답：D

설명：
The PI is responsible for ensuring that the source data is accurately recorded in the electronic Case Report Forms (eCRFs). This accurate transposition of data is critical to maintaining data integrity and ensuring that the data collected at the site is consistent with the reported clinical outcomes.
GCP guidelines specify that source data should be accurate, legible, and directly reflected in the CRFs to maintain consistency and reliability.
"The PI must ensure that the source data are accurately and completely recorded in the eCRFs to maintain data integrity." Objectives:
* Ensure accurate data transposition from source to CRF.
* Maintain high standards of data quality and reliability.

질문 # 73
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. Placebo-controlled
B. Blinding
C. Privacy controls
D. Randomization

정답：D

설명：
Randomization is a key element in open-label, parallel group clinical trials to reduce selection bias and ensure that participant allocation is not influenced by investigators. Despite the absence of blinding in open-label studies, randomization maintains the validity and reliability of the results by evenly distributing confounding factors between groups.
GCP guidelines recommend randomization as a core element in clinical trial design to ensure unbiased allocation of participants.
"Randomization in parallel group trials helps minimize selection bias and ensures the comparability of intervention groups." Objectives:
* Maintain scientific rigor through randomization.
* Minimize selection bias in clinical studies.

질문 # 74
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실없게 농담은, 이 사람은 대체 무슨 말을 하고 있는 걸까, ACRP ACRP-CP 덤프도 마찬가지 입니다, ACRP-CP덤프의 도움으로 여러분은 많은 시간과 돈을 들이지 않으셔도 혹은 학원등록을 하지 않으셔도 ACRP-CP덤프로 안전하게 시험을 통과하실 수 있습니다.덤프문제는 50문항으로 부터 1000문항 등 매 과목보다 문항수가 다른데 거의 2,3일이면 대부분 문제를 마스터 할수 있습니다.

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