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Certification for IRB Professionals (CIP) EXAM FULL QUESTIONS AND ANSWERS NEW UPDATE 2025 EDITION

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Certification for IRB Professionals (CIP) EXAM FULL QUESTIONS AND ANSWERS NEW UPDATE 2025 EDITION According to the Belmont Report, respect for persons usually demands that subjects... - Answers - enter into research voluntarily & with adequate information According to the Belmont Report, the moral requirement that there be fair outcomes in the selection of research subjects, expresses the principle of: - Answers - Justice A poorly designed protocol is considered unethical because... - Answers - research subjects may be put at risk or inconvenienced for insufficient reason When should an IRB suspend or terminate approval of research? - Answers - When it is not being conducted in accordance with the IRB's requirements A quorum for a convened IRB meeting requires the presence of... - Answers - a nonscientific member What is required in research involving no more than minimal risk with children? - Answers - Adequate provisions are made for assent of the child and permission of parent or guardian Federal regulations require each IRB to have written procedures for... - Answers - initial & continuing review of research and for reporting its findings and actions to the investigator and the institution What are the 3 ethical principles discussed in the Belmont Report? - Answers - Respect for Persons, Justice, & Beneficence An example of how the Principle of Beneficence can be applied to a study employing human subjects? - Answers - Determining that the study has a maximization of benefits & a minimization of risks. The researcher's failure to protect research subjects from deductive disclosure is the primary ethical violation of which study? - Answers - Harvard "Tastes, Ties, and Time (T3)" study ()" What is an example of how the principle of beneficence is applied to a study involving human subjects? - Answers - Ensuring that risks are reasonable in relationship to anticipated benefits 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: - Answers - Respect for Persons Which study is linked most directly to the establishment of the National Research Act in 1974 and ultimately to the Belmont Report and Federal regulations for human subject protection? - Answers - "The Public Health Service Tuskegee Study of Untreated Syphilis in the Negro Male" The Belmont Principle of beneficence requires that... - Answers - potential benefits justify the risks of harm 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? - Answers - 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. How long is an investigator required to keep consent documents, IRB correspondence, and research records? - Answers - For a minimum of three years after completion of the study According to federal regulations, when can the IRB use expedited review on a new, proposed study? - Answers - The study involves no more than minimal risk and meets one of the allowable categories of expedited review specified in federal regulations

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Certification for IRB Professionals (CIP)
EXAM FULL QUESTIONS AND
ANSWERS NEW UPDATE 2025 EDITION
According to the Belmont Report, respect for persons usually demands that subjects... -
Answers - ✔✔enter into research voluntarily & with adequate information

According to the Belmont Report, the moral requirement that there be fair outcomes in
the selection of research subjects, expresses the principle of: - Answers - ✔✔Justice

A poorly designed protocol is considered unethical because... - Answers - ✔✔research
subjects may be put at risk or inconvenienced for insufficient reason

When should an IRB suspend or terminate approval of research? - Answers - ✔✔When
it is not being conducted in accordance with the IRB's requirements

A quorum for a convened IRB meeting requires the presence of... - Answers - ✔✔a
nonscientific member

What is required in research involving no more than minimal risk with children? -
Answers - ✔✔Adequate provisions are made for assent of the child and permission of
parent or guardian

Federal regulations require each IRB to have written procedures for... - Answers -
✔✔initial & continuing review of research and for reporting its findings and actions to the
investigator and the institution

What are the 3 ethical principles discussed in the Belmont Report? - Answers -
✔✔Respect for Persons, Justice, & Beneficence

An example of how the Principle of Beneficence can be applied to a study employing
human subjects? - Answers - ✔✔Determining that the study has a maximization of
benefits & a minimization of risks.

The researcher's failure to protect research subjects from deductive disclosure is the
primary ethical violation of which study? - Answers - ✔✔Harvard "Tastes, Ties, and
Time (T3)" study (2006-2009)"

What is an example of how the principle of beneficence is applied to a study involving
human subjects? - Answers - ✔✔Ensuring that risks are reasonable in relationship to
anticipated benefits

, 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: - Answers - ✔✔Respect for
Persons

Which study is linked most directly to the establishment of the National Research Act in
1974 and ultimately to the Belmont Report and Federal regulations for human subject
protection? - Answers - ✔✔"The Public Health Service Tuskegee Study of Untreated
Syphilis in the Negro Male"

The Belmont Principle of beneficence requires that... - Answers - ✔✔potential benefits
justify the risks of harm

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? - Answers - ✔✔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.

How long is an investigator required to keep consent documents, IRB correspondence,
and research records? - Answers - ✔✔For a minimum of three years after completion of
the study

According to federal regulations, when can the IRB use expedited review on a new,
proposed study? - Answers - ✔✔The study involves no more than minimal risk and
meets one of the allowable categories of expedited review specified in federal
regulations

Amendments involving changes to IRB approved protocols do NOT need prior IRB
approval if: - Answers - ✔✔The changes must be immediately implemented for the
health and well-being of the subject.

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? - Answers - ✔✔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.

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? - Answers - ✔✔"Taking part

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