Irb and citi - Study guides, Class notes & Summaries

Social/Behavioral Research Training (CITI) Good Clinical Practice (GCP) - correct answer international ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects Clinical Trial (NIH Def) - correct answer Beyond just biomedical studies, Social and Behavioral interventions are now defined as clinical trials. Why implement GCP? - correct answer - Protect participants - Prevent non-compliance issues - Y...

CITI Training, Modules 1-24 (Biomedical Research) Questions and Answers 100% Pass The Belmont Report's principle of respect for persons incorporates at least two ethical convictions: first, that individuals should be treated as autonomous agents, and second, that: A. Persons with diminished autonomy should only participate in no more than minimal risk research. B. Persons with diminished autonomy should be excluded from research. C. Persons with diminished autonomy are entitled to prote...

CITI Training Questions And Answers Three principles of Belmont Report - ANS Respect for Persons Beneficence Justice The Belmont Report Principle of Beneficence - ANS MAXIMIZATION of benefits and MINIMIZATION of risks T/F Belmont Report indicates it is necessary to rigorously avoid conflicts of interest - ANS TRUE The Belmont Report Respect for Person - ANS Requires that subjects freely choose to participate in research (voluntariness) and that they are adequately inform...

CITI TRAINING COMPLETE QUESTIONS WITH 100% VERIFIED QUESTIONS An example of an institutional COI is: - ANS An industry sponsor pays for the construction of a new research laboratory at the organization The peer review process can create conflicts of interest because the choice of who reviews a potentially publishable project may show: - ANS There may be bias by the peer reviewer as to the area of research During an Institutional Review Board (IRB) meeting, any IRB member who may have ...

History and Ethical Principles - SBE CITI Training questions and Answers Scored A+ Which of the following are the three principles discussed in the belmont report? Respect for persons, beneficence, Justice Which of the following is an example of how the principle of beneficence can be applied to a study employing human subjects? Determining that the study has a maximization of benefits and minimization of risks All of the following are true regarding the belmont report except: ...

CITI Internet-Based Research SBE Latest Update Graded A+ What is a primary advantage of internet-based research? It allows for a broader, more diverse participant pool and greater flexibility in data collection. What challenges arise with participant verification in online studies? There is a risk of fraudulent responses due to the difficulty of verifying participant identity online. How does informed consent differ in internet-based research? Informed consent must be obtained...

CITI Training Exam Questions With Answers Updated Graded A+. Identify the following groups that are protected in the federal regulations (45 CFR 46), specifically in Subparts B, C, and D with additional protections: A. Pregnant women, prisoners, children B. Prisoners, children, and older adults C. Pregnant women, prisoners, and individuals who are economically disadvantaged D. Children, prisoners, and individuals who are critically ill Correct ans - A. Pregnant women, prisoners, children ...

CITI Training, Modules 1-24 (Biomedical Research) Questions and Answers (2023/2024) With Complete Solution. 1. The Belmont Report's principle of respect for persons incorporates at least two ethical convictions: first, that individuals should be treated as autonomous agents, and second, that: A. Persons with diminished autonomy should only participate in no more than minimal risk research. B. Persons with diminished autonomy should be excluded from research. C. Persons with diminished au...

CITI GCP Training Questions and Answers | Latest Version | 2024/2025 | 100% Verified The International Council for Harmonisation (ICH) guideline E6 has more extensive requirements for maintaining confidentiality of medical records and granting access to third parties compared to the FDA and HHS. According to the ICH E6 guideline, investigators must: Clearly disclose to participants in the informed consent form that the monitor, auditor, Institutional Review Board (IRB)/Independent ...

CITI IRB Populations and Unanticipated Problems