What do citi - Study guides, Class notes & Summaries

CITI IRB (Conflicts of Interest & Basics of Info Security);CITI training questions and answers 2023-2024 complete,100% verified and updated A researcher's membership on an advisory board with an organization sponsoring research can create a COI because: It may be difficult for the researcher to appear neutral, as the researcher may have an interest in the research's success During an Institutional Review Board (IRB) meeting, an IRB member who may have a potential COI with a study under re...

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 - 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 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 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 Review Questions With Complete Solutions Latest Update (Graded 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 th...

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 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 –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 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...