Citi Irb Regulations Answers

In: Science

Submitted By sls420
Words 553
Pages 3
Quiz Results - The Regulations - SBE
You correctly answered 5 of 5 and received 5 of 5 possible points.
Scroll down to review the quiz questions and the explanation of the answers.
Question 1
Question : According to the federal regulations, research is eligible for exemption, if
Your answer : The research falls into one of six categories of research activity described in the regulations.
Correct Answer : The research falls into one of six categories of research activity described in the regulations.
Comment : Research is only eligible for exemption if all the activity associated with the research fall into one of six categories of activities described in the federal regulations. The regulations do allow some research with children to be exempt (although institutional policy may not). The duration of the study and the experience of the investigator are not criteria for determining eligibility for exemption. Points Earned : 1
Question 2
Question : In addition to pregnant women, fetuses, and neonates, another subpart of the DHHS regulations provides additional protections for which of the following vulnerable populations?
Your answer : Prisoners.
Correct Answer : Prisoners.
Comment : Prisoners are provided additional protections in the DHHS regulations. The DHHS regulations do not have specific additional protections for the elderly, for students, or for persons whose decision-making capabilities are impaired. Investigators may consider and the IRB may require additional safeguards for these populations.
Points Earned : 1
Question 3
Question : According to federal regulations, the expedited review process may be used when the study procedures pose:
Your answer : No more than minimal risk and the research activities fall within regulatory categories identified as eligible.
Correct Answer : No more than minimal risk and the research activities fall…...

Similar Documents

Citi

...with many other major players in the banking industry have and still are currently being faced with numerous changes in regulations. Such as the Dodd-Frank Wall Street Reform and Consumer Protection Act, which seeks to limit the amount of risk that customers can take on. The act also implements strict liquidity, capital, and leverage ratio regulations for all companies in the financial service industry. The impact of this law could make Citi’s capacity for pursuing business opportunities much more difficult, along with higher penalties along with higher interest expenses. The Federal Reserve has stated it will begin enforcing the law in 2014. An important part of the Dodd-Frank Reform Act is called The Volcker Rule and has been a hot topic of debate over the past few months. The rule is meant to force strict limits on banks taking part in "proprietary trading", which means that they are betting the bank's money by speculative trading in financial instruments. Essentially the rule is trying to ban proprietary trading, which is how banks currently trade for a profit. Basel III which was developed by the Basel Committee on Banking Supervision is a set of restrictions that aim to toughen the regulation of the banking sector. In an attempt to progress the banking sector's ability to handle the volatility arising from financial and economic problems. This impacts Citi by diverting profits to capital, away from increasing dividends, and hence will lower the company’s Return on......

Words: 343 - Pages: 2

Citi Informed Consent Sbe Quiz Answers

...Question 1 Question : A therapist at a free university clinic treats elementary school children with behavior problems who are referred by a social service agency. She is also a doctoral candidate who proposes using data she has and will collect about the children for a case-based research project. Which of the following statements about parental permission is correct? Your answer : The parents of the children might feel pressure to give permission to the therapist to use their children's data so that she will continue to provide services to their children. Correct Answer : The parents of the children might feel pressure to give permission to the therapist to use their children's data so that she will continue to provide services to their children. Comment : When a care provider becomes a researcher, both the child clients and their parents may not feel free to choose not to participate in the provider's study. A researcher who is also a care provider needs to be very clear that a decision not to participate in a study, or to allow records to be used, will not affect the care provided in the future. The fact that the therapist has access to her clients' records as a clinician does not entitle her to use information in the records for research purposes without parental permission and child assent. A school authority's permission to conduct the research does not replace the need for permission or assent. Finally, the children's right to choose cannot be overridden in......

Words: 942 - Pages: 4

Citi Program

...and Federal regulations for human subject protection? Your answer : Stanford Prison Experiment (Zimbardo). Correct Answer : The Public Health Service Tuskegee Study of Untreated Syphilis in the Negro Male. Comment : Points Earned : 0 Question 2 Question : The Belmont principle of beneficence requires that: Your answer : Potential benefits justify the risks of harm. Correct Answer : Potential benefits justify the risks of harm. Comment : Points Earned : 1 Question 3 Question : Humphreys collecting data for the Tearoom Trade study under the pretense that he was a lookout is an example of a violation of the principle of: Your answer : Respect for persons. Correct Answer : Respect for persons. Comment : Humphreys collecting data for the Tearoom Trade study while posing as a lookout is an example of a violation of the principle of respect for persons. Respect for persons requires that subjects freely choose to participate in research (voluntariness) and that they are adequately informed about a study (informed consent). Points Earned : 1 Question 4 Question : According to the Belmont Report, the moral requirement that there be fair outcomes in the selection of research subjects, expresses the principle of: Your answer : Respect for persons. Correct Answer : Justice. Comment : Points Earned : 0 Question 5 Question : Which of the following is an example of how the principle of beneficence is applied to a study involving human subjects? Your answer......

Words: 3242 - Pages: 13

Citi Notes

...research has been recognized in several national reports on research integrity: * A report from the Institute of Medicine in 1989 specifically recommended that departments and research units should monitor the supervision and training of young scientists to insure that it is adequate. [8] * In 1992, a Panel on Scientific Responsibility and the Conduct of Research concluded that "Research mentors ... are responsible for defining, explaining, exemplifying, and requiring adherence to the value systems of their institutions." [9] * Similarly, a report in 2000 emphasized the importance of continued mentoring for postdoctoral researchers. [10] Responsible conduct is more than the desire to do the right thing or the reading of relevant regulations and publications. Trainees must also recognize the wide range of accepted practices, and that some of these practices may be preferable to others. Furthermore, trainees need to understand that acting responsibly depends on an appreciation that: * Standards can vary between and within disciplines. * Standards can change over time. * In some cases standards are not yet clearly articulated. For trainees to understand the varied and evolving nature of these standards, it is necessary that experienced researchers clearly convey their understanding of accepted practices in the conduct of research. ------------------------------------------------- The Ethics of Mentoring Because of the inherent imbalance of power......

Words: 25741 - Pages: 103

Citi Quiz

...Question 1 Multiple Choice/Single Answer - Select only one answer A therapist at a free university clinic treats elementary school children with behavior problems who are referred by a social service agency. She is also a doctoral candidate who proposes using data she has and will collect about the children for a case-based research project. Which of the following statements about parental permission is correct? The superintendent of the school system can give permission for children to be in the study; therefore, the therapist doesn't have to ask the parents for permission. The therapist creates her clients' records; therefore, she does not need parents' permission to use the information for research purposes. The parents of the children might feel pressure to give permission to the therapist to use their children's data so that she will continue to provide services to their children. If it is the best interests of the community that the children participate in the study, parental permission is optional. Question 2 Multiple Choice/Single Answer - Select only one answer A general requirement for informed consent is that no informed consent may include any exculpatory language. Exculpatory language is that which waives or appears to waive any of the subject's legal rights or releases or appears to release those conducting the research from liability for negligence. Which of the following statements in a consent form is an example of exculpatory language? ......

Words: 711 - Pages: 3

The Regulations

...Question 1 Multiple Choice/Single Answer - Select only one answer According to the federal regulations, research is eligible for exemption, if The research falls into one of six categories of research activity described in the regulations. Participation in the research will involve 10 minutes or less of the subjects' time. The investigator is experienced in the field of inquiry. All the subjects are adults and the risk is minimal. Question 2 Multiple Choice/Single Answer - Select only one answer In addition to pregnant women, fetuses, and neonates, another subpart of the DHHS regulations provides additional protections for which of the following vulnerable populations? The elderly. Prisoners. Adults with decisional impairments. College students. Question 3 Multiple Choice/Single Answer - Select only one answer According to federal regulations, the expedited review process may be used when the study procedures pose: A minor increase over minimal risk and the sponsor needs approval before the next IRB meeting. No more than minimal risk and the research activities fall within regulatory categories identified as eligible. More than minimal risk, but the study replicates previously approved research. Any level of risk, but all the subjects are adults. Question 4 Multiple Choice/Single Answer - Select only one answer Continuing review of an approved and ongoing protocol Is not required unless additional risks have been identified. Is......

Words: 303 - Pages: 2

Quiz Results - Basic Institutional Review Board (Irb) Regulations and Review Process

...Quiz Results - Basic Institutional Review Board (IRB) Regulations and Review Process You correctly answered 3 of 5 and received 3 of 5 possible points. Scroll down to review the quiz questions and the explanation of the answers. Question 1 Question : | A subject in a clinical research trial experiences a serious, unanticipated adverse drug experience. How should the investigator proceed, with respect to the IRB, after the discovery of the adverse event occurrence? | Your answer : | Report the adverse drug experience in a timely manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism provided by the IRB. | Correct Answer : | Report the adverse drug experience in a timely manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism provided by the IRB. | Comment : | The most appropriate action for the investigator to take is to report the adverse drug experience in a timely manner using the forms provided by the institution. | Points Earned : | 1 | Question 2 Question : | How long is an investigator required to keep consent documents, IRB correspondence, and research records? | Your answer : | For a minimum of three years after completion of the study | Correct Answer : | For a minimum of three years after completion of the study | Comment : | Research investigators are responsible for retaining signed consent documents, IRB correspondence, and research records for at least three......

Words: 662 - Pages: 3

The Regulation

...Choice/Single Answer - Select only one answerAccording to the federal regulations, research is eligible for exemption, if | The investigator is experienced in the field of inquiry. The research falls into one of six categories of research activity described in the regulations. All the subjects are adults and the risk is minimal. Participation in the research will involve 10 minutes or less of the subjects' time. | Question 2 Multiple Choice/Single Answer - Select only one answerIn addition to pregnant women, fetuses, and neonates, another subpart of the DHHS regulations provides additional protections for which of the following vulnerable populations? | College students. The elderly. Adults with decisional impairments. Prisoners. | Question 3 Multiple Choice/Single Answer - Select only one answerAccording to federal regulations, the expedited review process may be used when the study procedures pose: | A minor increase over minimal risk and the sponsor needs approval before the next IRB meeting. Any level of risk, but all the subjects are adults. No more than minimal risk and the research activities fall within regulatory categories identified as eligible. More than minimal risk, but the study replicates previously approved research. | Question 4 Multiple Choice/Single Answer - Select only one answerContinuing review of an approved and ongoing protocol | Is limited to review of unanticipated problems. Must be conducted by a convened IRB. Is not......

Words: 298 - Pages: 2

Basic Institutional Review Board (Irb) Regulations

...human subject protection regulations that govern the participation of human volunteers in research in the United States. Learning Objectives By end of the module you should be able to: * Describe the role, authority, and composition of the IRB. * List the IRB requirements for conducting research involving human subjects. * Describe the types of IRB review. * Describe the process of working with the IRB. * Identify other regulations and regulatory groups that require compliance based on the type of research being conducted. IRB Role, Authority, and Composition The Role of the IRB An Institutional Review Board (IRB) is a review committee established to help protect the rights and welfare of human research subjects. Regulations require IRB review and approval for research involving human subjects if it is funded or regulated by the federal government. Most research institutions, professional organizations, and scholarly journals apply the same requirements to all human research. Although federal regulations refer to IRBs, an institution may have chosen a different name for this committee. To clarify when IRB review is required, let's define some terms: * Research: Federal regulations define research as: "a systematic investigation... designed to develop or contribute to generalizable knowledge." [45 CFR 46.102(d)] If an investigator is unclear about whether a planned activity is research, the investigator should contact his/her IRB office. * ......

Words: 5929 - Pages: 24

Citi

...Question 1 Question : According to the federal regulations, research is eligible for exemption, if Your answer : The research falls into one of six categories of research activity described in the regulations. Correct Answer : The research falls into one of six categories of research activity described in the regulations. Comment : Research is only eligible for exemption if all the activity associated with the research fall into one of six categories of activities described in the federal regulations. The regulations do allow some research with children to be exempt (although institutional policy may not). The duration of the study and the experience of the investigator are not criteria for determining eligibility for exemption. Points Earned : 1 Question 2 Question : In addition to pregnant women, fetuses, and neonates, another subpart of the DHHS regulations provides additional protections for which of the following vulnerable populations? Your answer : Prisoners. Correct Answer : Prisoners. Comment : Prisoners are provided additional protections in the DHHS regulations. The DHHS regulations do not have specific additional protections for the elderly, for students, or for persons whose decision-making capabilities are impaired. Investigators may consider and the IRB may require additional safeguards for these populations. Points Earned : 1 Question 3 Question : According to federal regulations, the expedited review process may be......

Words: 522 - Pages: 3

Citi

...to sign consent forms linking them to a study about illegal activities could put them at risk of harm. The federal regulations provide sufficient flexibility to address some of these concerns, particularly for research posing no more than minimal risk of harm. For example, the regulations allow waivers of and alterations in the requirements for the consent and documentation processes. Learning Objectives By the end of this module you should be able to: • Distinguish between consent as a process and the documentation of consent. • Recognize the elements of consent. • Determine when waivers are appropriate. • Identify methods for ensuring comprehension of consent. Overview of Informed Consent Federal regulations require researchers to obtain legally effective informed consent from the subject or the subject's legally authorized representative (LAR). There are two parts to informed consent. The first is the process of providing information to prospective subjects. The second is documentation that the process took place and is a record of the subjects' agreement to take part in the study. In practice, informed consent forms often are used as a means to provide information about a study, and, when signed, serve as documentation of consent. However, in some cases, an oral consent process without documentation may be approved by an Institutional Review Board (IRB). The Process Informed consent is a process that begins with the recruitment and screening of a subject and......

Words: 2868 - Pages: 12

Citi Training Exam Results

...respect to the IRB, after the discovery of the adverse event occurrence? Your answer : Report the adverse drug experience as part of the continuing review report. Correct Answer : Report the adverse drug experience in a timely manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism provided by the IRB. Comment : The most appropriate action for the investigator to take is to report the adverse drug experience in a timely manner using the forms provided by the institution. Points Earned : 0 Question 2 Question : How long is an investigator required to keep consent documents, IRB correspondence, and research records? Your answer : For a minimum of three years after completion of the study Correct Answer : For a minimum of three years after completion of the study Comment : Research investigators are responsible for retaining signed consent documents, IRB correspondence, and research records for at least three years after completion of the research. Since research records are property of the institution, local institutional policy or sponsoring agency requirements may dictate these records are kept longer. The sponsor and the IRB office should be contacted to make sure that the minimum of three years meets their requirements. Points Earned : 1 Question 3 Question : According to federal regulations, which of the following best describes when expedited review of a new, proposed study may be used by the IRB? Your answer : The study is...

Words: 611 - Pages: 3

Regulation Answer

...- The Regulations - SBE You correctly answered 5 of 5 and received 5 of 5 possible points. Scroll down to review the quiz questions and the explanation of the answers. Question 1 Question : According to the federal regulations, research is eligible for exemption, if Your answer : The research falls into one of six categories of research activity described in the regulations. Correct Answer : The research falls into one of six categories of research activity described in the regulations. Comment : Research is only eligible for exemption if all the activity associated with the research fall into one of six categories of activities described in the federal regulations. The regulations do allow some research with children to be exempt (although institutional policy may not). The duration of the study and the experience of the investigator are not criteria for determining eligibility for exemption. Points Earned : 1 Question 2 Question : In addition to pregnant women, fetuses, and neonates, another subpart of the DHHS regulations provides additional protections for which of the following vulnerable populations? Your answer : Prisoners. Correct Answer : Prisoners. Comment : Prisoners are provided additional protections in the DHHS regulations. The DHHS regulations do not have specific additional protections for the elderly, for students, or for persons whose decision-making capabilities are impaired. Investigators may consider and the IRB may......

Words: 283 - Pages: 2

Citi

...------------------------------------------------- Choose a security question and answer. Enter your name as you are known at UHCL. Enter your choice of email address. Number 6 – DO NOT choose CME/CEU credits unless you know that you need them for your professional certification. Students will unlikely ever need this option. It does not cost individuals who are affiliated with UHCL to take the CITI Laboratory Animal Welfare training. Number 7 – Most will choose “No, I am not interested at any price.” Please note that UHCL is not responsible for the cost of study guides. Number 8 – It is your choice. ------------------------------------------------- Fill in fields that have an asterisk. Faculty and professional staff should choose “Principal Investigator” or “CPHS Member” depending on role. Students should choose “Student Researcher” and either “Graduate Level” or “Undergraduate.” Non-researchers should choose a title that best describes their role (Research Administrator, etc.). Other fields are optional. ------------------------------------------------- For Human Subjects Researchers: On Question 1, choose “Social & Behavioral Research” Course. On Question 2, leave it blank. On Question 3, choose “Not at this time, thank you.” ------------------------------------------------- You will have the following required courses to take. To start a course, click “Enter.” Module 1: History and Ethical Principles – SBR Module 2: The......

Words: 636 - Pages: 3

Irb Collaboration

...A Michael Tarver ID: 5548861 Log Out Help CITI Program Collaborative Institutional Training Initiative at the University of Miami Search Knowledge Base Search Main Menu My Profiles My CEUs My Reports Support Main Menu › Quiz Basic Institutional Review Board (IRB) Regulations and Review Process Basic Institutional Review Board (IRB) Regulations and Review Process Quiz Instructions: Please provide an answer for all questions. Each question is one point. Click on the Submit button to register your answers. After submitting your answers, the correct answer to each question and an explanation will be displayed. Navigational links to the next module will be provided. All quiz questions count towards your score. You should answer all questions. Question 1 Multiple Choice/Single Answer - Select only one answer A subject in a clinical research trial experiences a serious, unanticipated adverse drug experience. How should the investigator proceed, with respect to the IRB, after the discovery of the adverse event occurrence? Report the adverse drug experience to the IRB only if there are several other occurrences. Report the adverse drug experience in a timely manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism provided by the IRB. Report the adverse drug experience as part of the continuing review report. Do not report the adverse drug experience to the IRB since it is a common adverse......

Words: 492 - Pages: 2

Kuroko no Basket Movie 3: Winter Cup Soushuuhen - Tobira no Mukou (2016) | Space Bear and the Love Bomb | Скачать APK