100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
CITI Training| 120 questions| with complete solution $10.49   Add to cart

Exam (elaborations)

CITI Training| 120 questions| with complete solution

 4 views  0 purchase
  • Course
  • Institution

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 interes...

[Show more]

Preview 2 out of 12  pages

  • October 3, 2022
  • 12
  • 2022/2023
  • Exam (elaborations)
  • Questions & answers
avatar-seller
CITI Training| 120 questions| with complete solution
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 choose to participate in
research (voluntariness) and that they are adequately informed about a study (informed consent)

The Belmont Report defines and delineates... Correct Answer: "Practice" and "Research"

The Belmont Report
The Principle of Justice Correct Answer: Research benefit and burden distribution and that
selection of subjects is fair.

T/F
The Belmont report describes the necessity to effectively manage conflicts of interest Correct
Answer: FALSE

Students in Research
The history of ethical regulations in human subjects research began with the Correct Answer:
Nuremberg Code

Nuremberg Code Correct Answer: Human subjects research guidelines and regulations

Year of the Nuremberg Code Correct Answer: 1949

Additional resources regarding IRB approval process Correct Answer: Faculty advisor/Research
Mentor
IRB office
Human subjects research websites

What element must be included in an informed consent? Correct Answer: All foreseeable risks
and discomforts

Which type of IRB review does not require and IRB approval but DOES require a Determination
by the IRB? Correct Answer: If the study qualifies for EXEMPTION

, Another name for the "Exempt" status Correct Answer: the Common Rule
stated in Title 45 Part 46 Subpart A

How can faculty researchers avoid coercion of student subjects? Correct Answer: Avoid using
their own students in their research

Name the type of Review: Research study that involves use of educational tests, survey,
interviews, or observations of public behavior without identifiable information. Correct Answer:
Exempt Review category 2

Name the type of review: A study involving data collected that could have an impact on human
subject's careers and it contains identifiers of the subjects. Correct Answer: Full Board Review

Type of review that qualifies if no identification of subjects and/or their responses would
reasonably place them at risk of criminal or civil liability or be damaging to the subjects financial
standing, employability, insurability, reputation, or be stigmatizing, unless reasonable and
appropriate protections will be implemented so that risks related to invasion of privacy and
breach of confidentiality are no greater than minimal Correct Answer: Expedited review

Type of review: data that is collected does not meet definition of human subjects research as
stated by federal regulations. No info ABOUT human ie. info about a business Correct Answer:
Not Human Subjects

Federal regulations define human subjects as "living individual about whom an investigator
conducting research obtains"...? (2 components) Correct Answer: "1.data through intervention or
interaction with the individual
2. identifiable private information"

Name the 3 responsibilities the IRB is charged with Correct Answer: 1. Protecting the rights and
welfare of human subjects
2. Assuring that all applicable institutional policies and federal regulations related to research
with human subjects are followed
3. Reviewing subject recruitment materials and strategies

T/F
IRB's investigate scientific misconduct Correct Answer: False

T/F
IRB's do not review manuscripts prior to submission for publication Correct Answer: True

DHHS
FDA Correct Answer: Depts. IRB's review for current policies
-Department of Health and Human Services
-Food and Drug Administration

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller Classroom. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for $10.49. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

80467 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy study notes for 14 years now

Start selling
$10.49
  • (0)
  Add to cart