What do citi - Study guides, Class notes & Summaries

CITI Exam Review Questions and answers, VERIFIED/ What is the main risk of harm in big data research characterized as? - -Informational Which of the following is an example of big data use in research? - -A study examines social interactions by combing different datasets (social media data from Facebook and geolocation data from an app) Big data can be: - -Predictive, Prescriptive, descriptive Which of the following is a general consideration for IRBs reviewing big data research? - -Th...

CITI Training Exam Questions and Answers 100% Correct Three principles of Belmont Report - Correct Answer ️️ -Respect for Persons Beneficence Justice The Belmont Report Principle of Beneficence - Correct Answer ️️ -MAXIMIZATION of benefits and MINIMIZATION of risks T/F Belmont Report indicates it is necessary to rigorously avoid conflicts of interest - Correct Answer ️️ -TRUE The Belmont Report Respect for Person - Correct Answer ️️ -Requires that subjects freely choos...

CITI Training 134 Questions With Complete Solutions Latest Updated 2024 (GRADED A+) What must you file before conducting human clinical trials with an experimental drug? Correct Answer: IND application (Form FDA 1571) During the clinical development phase of the IND process, what must sponsors do? Correct Answer: Maintain current IND application by amending IND with new Form FDA 1571 and providing FDA with: safety updates copies of new protocols FDA 1572 Annual Progress reports this doc...

CITI Training 134 Questions With Complete Solutions Latest Update Score A+. What must you file before conducting human clinical trials with an experimental drug? Correct Answer: IND application (Form FDA 1571) During the clinical development phase of the IND process, what must sponsors do? Correct Answer: Maintain current IND application by amending IND with new Form FDA 1571 and providing FDA with: safety updates copies of new protocols FDA 1572 Annual Progress reports this document n...

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 –Social & Behavioral Research, Exam Review Questions and answers, rated A+ What procedures must be described in an agreement called an "assurance of compliance" with OHRP? - -Procedures in place that ensure that subjects will be protected in a manner commensurate with the Common Rule, including review by an independent committee comparable to an IRB. A researcher proposes to conduct a study at a foreign site that has been determined to be exempt from the federal regulations b...

CITI RCR- Using Animals In Research Questions and Answers Graded A+ Prior to implementing any significant change in the use of animals, what is the most important thing that the research team must do? Obtain IACUC approval for the change. What is the primary purpose of the "3Rs" concept from Russell and Burch? To decrease the use of animals in research and to minimize pain and distress caused by animal experiments. Which entity is responsible for monitoring institutional compliance...

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 2023 Exam Questions with Correct Answers Privacy, in the health information context, refers to: - Answer-The rules about who can access health information, and under what circumstances. In the U.S., privacy protections for health information come from: - Answer-Federal, state, local, and private certification organizations' requirements With respect to permissions for uses and disclosures, HIPAA divides health information into three categories. Into which category do discussions w...

Module 3 Exam (CITI) - Questions with 100% Correct Answers Data are made anonymous by -Destroying all identifiers connected to the data. -Requiring all members of the research team to sign confidentiality agreements. -Keeping the key linking names to responses in a secure location. -Reporting data in aggregate form in publications resulting from the research. In a longitudinal study that will follow children from kindergarten through high school and will collect information about illegal activ...