Citi 1 exam questions - Study guides, Class notes & Summaries

Which of the following studies would need IRB approval? - Studies collecting identifiable information about living individuals. Identify one way faculty researchers can possibly avoid undue influence of student subjects? - Avoid recruiting their own students in the research Under the U.S. Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) regulations, what is the Institutional Review Board (IRB) charged with? Select all that apply. - - Protecting the ...

Which of the following studies would need IRB approval? - Studies collecting identifiable information about living individuals. Identify one way faculty researchers can possibly avoid undue influence of student subjects? - Avoid recruiting their own students in the research Under the U.S. Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) regulations, what is the Institutional Review Board (IRB) charged with? Select all that apply. - - Protecting the ...

CITI Training Review: Human Subjects Research Exam Questions And Answers Example of how the principle of beneficence is applied to a study involving human subjects - ANS Ensuring that the risks are reasonable in relationship to anticipated benefits Harvard "Tastes, Ties, and Time (T3)" () Study involves this primary ethical violation - ANS The researcher's failure to protect research subjects from deductive disclosure (primary ethical violation) "The Public Health Service Tuskegee St...

CITI - HIPAA Training Exam Questions and Answers 100% Pass In the US, privacy protections for health information come from: - Answer- Privacy protections come from all of these sources - both federal and state law, as well as the requirements of private certification organizations. Privacy, in the health information context discussed here, refers to: - Answer- The rules about who can access health information, and under what circumstances. Under the federal HIPAA regulations, state health...

CITI Training Exam Questions With Complete Solutions Latest Update (Score A+). What is the timeline of drug development? Correct Answer: Preclinical trials, IND Submission, Clinical Development (Phase I-III), NDA submission, Marketing (Phase IV) When does a sponsor submit the IND? Correct Answer: Prior to clinical development phases (human trials). *30 day process. What is the NDA? Correct Answer: New Drug Application, submitted prior to Phase IV marketing phase. How long does the NDA su...

CITI Modules 2023 Exam Questions with Correct Answers 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: - Answer-Persons with diminished autonomy are entitled to protection. Which of the following are the three principles discussed in the Belmont Report? - Answer-Respect for Persons, Beneficence, Justice Which of the following is an example of how the pr...

CITI EXAM INFO MODULES 1-3 QUESTIONS WITH CORRECT ANSWERS

CITI Training: Revised Common Rule. Exam Review Questions and answers, rated A+ Which of the following is accurate regarding electronic signatures? - -Specifically allowed by the Final Rule The Final Rule added the requirement that: - -Key information essential to decision making receive priority by appearing at the beginning of the consent document and being presented first in the consent discussion. Research approved on 1 September 2019 conducted by a regulated entity would be sub...

CITI Training Exam Questions and answers, rated A+/ Americans with Disabilities Act - -Established in 19990, helps ensure people with disabilities have the same rights and opportunities as other Americans. ADA National Network - -Provides training resources for those seeking to address this issue Animals cannot give informed consent - -What is a dilemma faced in using animals for research? 1. Health Research Extension Act of 1985 2. Ethical and scientific principles in the U.S. Governme...