Table of Contents

Which of the following is true regarding authors who seek to publish the same content?

Which of the following is true regarding authors who seek to publish the same content in multiple papers? Using the same content in multiple papers is deceptive if it is not properly disclosed to journal editors or other relevant entities.

What is true regarding research misconduct?

Which of the following is true regarding research misconduct? Falsification involves purposefully manipulating research materials, equipment, or processes, or changing or omitting data or results such that the research is not accurately represented in the research record.

What is the primary criterion for authorship?

The ICMJE recommends that authorship be based on the following 4 criteria: Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; AND. Drafting the work or revising it critically for important intellectual content; AND.

Which author is normally responsible for sharing reprints of a publication with readers?

Comment : The corresponding author is normally responsible for sharing reprints of a publication with readers.

What is the responsibility of each author?

“Each author is expected to have made substantial contributions to the conception OR design of the work; OR the acquisition, analysis, OR interpretation of data; OR have drafted the work or substantively revised it; AND to have approved the submitted version (and any substantially modified version that involves the …

Which author is normally responsible?

Your answer : The author who has made the most significant contribution. Correct Answer : The corresponding author. Comment : The corresponding author is normally responsible for sharing reprints of a publication with readers.

What is the main function of the Bayh Dole Act of 1980?

The Bayh-Dole Act, formerly known as the Patent and Trademark Act Amendments, is a federal law enacted in 1980 that enables universities, nonprofit research institutions and small businesses to own, patent and commercialize inventions developed under federally funded research programs within their organizations.

What are the three main goals of data lifecycle management?

The three main goals of data life cycle management are CONFIDENTIALITY, AVAILABILITY AND INTEGRITY.

Which of the following is the main reason why proper training in euthanasia?

Which of the following is the main reason why proper training in euthanasia techniques is important? Improper techniques can cause unnecessary pain and distress in animals. To decrease the use of animals in research and to minimize pain and distress caused by animal experiments.

Which of the following is the clearest example of Macroethical issue?

Which of the following is the clearest example of a macroethical issue? Balancing risks and benefits from nanotechnology research.

Which of the following is an example of how the principle of beneficence can be applied?

Which of the following is an example of how the principle of beneficence can be applied to a study employing human subjects? Determining that the study has a maximization of benefits and a minimization of risks. The Belmont principle of beneficence requires that: Potential benefits justify the risks of harm.

Which is an example of a situation where deferential vulnerability might be a factor?

Examples might include young children, or adults with cognitive impairments that affect decision making. 2. Situational cognitive vulnerability – subjects do not lack capacity, but are in situations that do not allow them to exercise their capacities effectively.

What are inducements in research?

Page 35. Undue Inducement. “Payment in money or in kind to research. subjects should not be so large as to persuade them to take undue risks or volunteer against their better judgment. Payments or rewards that undermine a person’s capacity to exercise free choice invalidate consent.”

What is the term for management controls that are built in to a research study for example independent data analysis )?

What is the term for management controls that are built in to a research study (for example, independent data analysis)? Inherent controls. An example of an individual financial COI is: A researcher’s wife holds equity in a publicly traded pharmaceutical company that is also the sponsor of the researcher’s study.

What statement about risks in social and behavioral sciences research is most accurate?

What statement about risks in social and behavioral sciences research is most accurate: Risks are specific to time, situation, and culture. The primary purpose of a Certificate of Confidentiality is to: Protect identifiable research information from compelled disclosure.

What is an expedited review?

Expedited review involves a review of a proposal by a subset of the IRB that includes the Chair and at least one other board member. Expedited review does not mean a quick review; the IRB determined whether a project requires expedited or full review.

What is the primary purpose of a certificate of confidentiality?

Certificates of Confidentiality are issued by the National Institutes of Health (NIH) and other HHS agencies to protect identifiable research information from forced or compelled disclosure.

Can investigator B use the specimens for cancer research without re consent if the specimens are de identified?

Can Investigator B use the specimens for cancer research without re-consent if the specimens are de-identified? Yes, if the biospecimens are de-identified then the research is no longer considered human subjects research.

What is an appropriate method for maintaining confidentiality of private information?

What is an appropriate method for maintaining confidentiality of private information obtained from human subjects? Keeping data in a password-protected database. Storing data in a secured cabinet. Coding data or specimens and keeping the key to the code in a separate location.

For which types of studies must consent forms be posted on a public web site?

Clinical Trial Informed Consent Form Posting (45 CFR 46.116(h)) The revised Common Rule requires that for any clinical trial conducted or supported by a Common Rule department or agency, one consent form be posted on a publicly available federal website within a specific time frame.