便利なACRP ACRP-CP練習問題 &合格スムーズACRP-CP対策学習 |信頼的なACRP-CP過去問

私たちは皆、ほとんどの候補者が製品の品質を心配することを知っていました。ACRP-CP学習教材の品質を保証するために、会社のすべての労働者は、共通の目標のために、 ; ACRP-CP試験問題です。 ACRP-CPガイドトレントを購入すると、高品質の製品、リーズナブルな価格、アフターサービスを提供することが保証されます。私たちのACRP-CPテストトレントは、他の学習教材よりもあなたにとってより良い選択だと思います。

10年以上のビジネス経験により、当社のACRP-CPテストトレントは、顧客の購入体験を非常に重要視していました。電子製品の購入速度を心配する必要はありません。弊社では、ACRP-CP試験準備の信頼性を長期間にわたって評価および評価し、保証された購入スキームを提案するために尽力しています。必要な場合は、ACRP-CPテストトレントを使用するためのリモートオンラインガイダンスも利用できます。通常、購入後数分でACRP-CP練習問題を効率よく取得できます。

>> ACRP-CP練習問題 <<

ACRP-CP対策学習、ACRP-CP過去問

資格証明書を使用すると、この専門職に就く資格が得られます。したがって、テストACRP-CP認定を取得することは、将来の雇用にとって極めて重要です。また、ACRP-CP学習ツールは、短時間でACRP-CPテストを取得したいユーザーに優れた学習プラットフォームを提供できます。弊社を信頼することを選択できる場合、ACRP-CPスタディガイドを使用すると良い経験が得られ、試験に合格し、テストACRP-CP認定で良い成績を得ることができると思います。

ACRP Certified Professional Exam 認定 ACRP-CP 試験問題 (Q65-Q70):

質問 # 65
A PI is reviewing the CRF for a recent subject visit and notices the participant's heart rate and temperature are not recorded. Which of the following study documentation practices was neglected?

A. Original
B. Contemporaneous
C. Attributable
D. Complete

正解：D

解説：
The missing data indicates a lack of completeness in the study documentation. Completeness is a fundamental requirement in clinical trials, as all necessary information must be recorded accurately and in full. Missing vital signs such as heart rate and temperature can compromise the validity of the data and affect the study's outcomes.
GCP guidelines state that all data collected during the study must be complete, accurate, and consistent with source documents.
"Clinical trial documentation must be complete, containing all data as required by the protocol toensure data integrity." Objectives:
* Ensure comprehensive data recording.
* Maintain accuracy and completeness in study records.

質問 # 66
Prior to initiation of a clinical trial, review by an IRB/IEC is required for which of the following documents?

A. Protocol, IB, and information about payments and compensation available to subjects
B. Protocol, informed consent, and clinical trial agreement
C. IB, site coordinator CVs, and information about payments and compensation available to subjects
D. Protocol, site coordinator CVs, and clinical trial agreement

正解：A

解説：
Before a clinical trial can begin, the IRB/IEC must review the protocol, Investigator's Brochure (IB), and any information related to payments and compensation. This review ensures that the study is ethically sound, scientifically valid, and that participants are informed about any financial considerations.
GCP guidelines specify that essential documents, including the protocol, IB, and compensation details, must be reviewed by the IRB/IEC to maintain ethical oversight.
"The IRB/IEC must evaluate the protocol, IB, and any financial disclosures to ensure ethical compliance and participant protection." Objectives:
* Guarantee ethical oversight in clinical trial conduct.
* Protect participants through informed consent and transparency.

質問 # 67
The objective of a randomized clinical trial is to look at whether an IP is effective in preventing recurrence of a disease. What would be a possible primary endpoint of the trial?

A. Use of concomitant medications to treat the symptoms
B. Impact of an approved vaccine against the disease
C. Occurrence of known side effects of the IP
D. Time to occurrence of symptoms of the disease

正解：D

解説：
In a clinical trial aimed at assessing whether an IP prevents disease recurrence, the primary endpoint would typically be the "time to occurrence of symptoms" indicating a relapse or recurrence. This endpoint directly measures the IP's effectiveness in prolonging the symptom-free period.
This answer follows the GCP guideline, which states that primary endpoints should directly reflect the trial's objectives, particularly when evaluating recurrence prevention.
"In trials evaluating recurrence prevention, the primary endpoint should measure the time until recurrence of the target symptoms or condition." Objectives:
* Assess the efficacy of IP in preventing disease recurrence.
* Accurately measure the time to recurrence as a primary endpoint.

質問 # 68
A study sponsor approaches a facility about participating in their research study. The study sponsor requires use of social media as its sole method of recruitment. The site knows their institutional IRB/IEC does not approve of social media recruiting. How should the site respond?

A. Decline the study.
B. Use a central IRB/IEC.
C. Recruit for the study without use of social media.
D. Rely on the sponsor to notify the IRB/IEC.

正解：A

解説：
If the IRB/IEC has a policy that does not permit social media recruiting, the site must adhere to these regulations. Proceeding with a method not approved by the IRB/IEC would violate compliance requirements, so declining the study is the correct course of action.
The answer aligns with IRB/IEC regulations that prioritize ethical and compliant recruitment methods.
"Sites must follow the recruitment methods approved by their IRB/IEC to maintain compliance and ethical standards." Objectives:
* Adhering to ethical recruitment practices.
* Maintaining compliance with IRB/IEC policies.

質問 # 69
Which of the following documents is maintained by a PI to ensure compliance with sponsor requirements?

A. A monitoring report that identifies deviation from the approved protocol.
B. Regulatory submission of protocol and accompanying documents to relevant regulatory authority.
C. Training records of site personnel on study protocol, and their study-related duties and functions.
D. A monitoring plan that is tailored to the specific human subject protection and data integrity risks of the trial.

正解：C

解説：
The PI is responsible for maintaining training records of site personnel, which demonstrate compliance with the sponsor's requirements for conducting the trial. Proper documentation of training ensures that all team members are knowledgeable about the protocol and study procedures.
GCP guidelines mandate that the PI maintains adequate records to demonstrate that all personnel involved in the study are properly trained and qualified.
"Training records of site personnel must be maintained to verify that the team is adequately trained on the protocol and their specific responsibilities." Objectives:
* Maintain training compliance.
* Document personnel qualifications for quality assurance.

質問 # 70
......

ACRPのACRP-CP認定試験はIT業界の中でとても普遍的な試験になります。試験の準備は時間とエネルギーがかかります。時は金なり社会に時間を無駄しないようによいツルを探し出されるのはみんなの希望です。It-PassportsのACRPのACRP-CP認証試験の問題集は君の20時間だけかかりますよ。

ACRP-CP対策学習: https://www.it-passports.com/ACRP-CP.html

当社のACRP-CP学習教材を購入したこれらの人々を支援するために、当社が提供するACRP-CP学習教材の更新と更新を担当する当社の専門家チームがあります、ACRP ACRP-CP練習問題不思議だと思っていますか、我々のACRP-CP練習問題を購入するだけで、認定試験に合格するのは簡単で、より良い自由な人生が来ています、ACRP ACRP-CP練習問題 1.直接情報を取得します、ACRP-CP学習ガイドの助けを借りて、多くの人々が労働市場で適切な仕事を得ることができます、ACRP-CPの合格率は98％以上です、ACRP ACRP-CP練習問題私たちは、衝動買いは後悔することは容易であることを知っていますから、あなたはご購入の前にやってみるのを薦めます。

資料として保存しておいていただきたい、中秋であり、空気も澄んでいる、当社のACRP-CP学習教材を購入したこれらの人々を支援するために、当社が提供するACRP-CP学習教材の更新と更新を担当する当社の専門家チームがあります。

素晴らしいACRP-CP練習問題一回合格-検証するACRP-CP対策学習

不思議だと思っていますか、我々のACRP-CP練習問題を購入するだけで、認定試験に合格するのは簡単で、より良い自由な人生が来ています、1.直接情報を取得します、ACRP-CP学習ガイドの助けを借りて、多くの人々が労働市場で適切な仕事を得ることができます。

Sean Stone Sean Stone

السيرة الذاتية

便利なACRP ACRP-CP練習問題 &合格スムーズACRP-CP対策学習 |信頼的なACRP-CP過去問

ACRP-CP対策学習、ACRP-CP過去問

ACRP Certified Professional Exam 認定 ACRP-CP 試験問題 (Q65-Q70):

素晴らしいACRP-CP練習問題一回合格-検証するACRP-CP対策学習

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