100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
Previously searched by you
Previously searched by you
logo
CITI Federal Regulations SBE Questions and Answers Rated A+ £8.13   Add to cart
Quickly navigate to
Preview
  2.  
  3. CITI Federal Regulations SBE
  4.  
  5. CITI Federal Regulations SBE

Exam (elaborations)

CITI Federal Regulations SBE Questions and Answers Rated A+
 8 views  0 purchase
  • Module
  • CITI Federal Regulations SBE
  • Institution
  • CITI Federal Regulations SBE

CITI Federal Regulations SBE Questions and Answers Rated A+ What is the purpose of the Common Rule in human subjects research? The Common Rule provides ethical guidelines and regulations to ensure the protection of human subjects involved in research. When is it necessary to obtain infor...

[Show more]

Preview 3 out of 20  pages

Document information

  • October 16, 2024
  • 20
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers

Subjects

  • citi federal regulations sbe questions and answer

Written for

  • CITI Federal Regulations SBE
  • CITI Federal Regulations SBE

Seller

avatar-seller
StellarScores

Reviews received

Content preview

CITI Federal Regulations SBE Questions
and Answers Rated A+

What is the purpose of the Common Rule in human subjects research?


✔✔The Common Rule provides ethical guidelines and regulations to ensure the protection of

human subjects involved in research.




When is it necessary to obtain informed consent from research participants?


✔✔Informed consent must be obtained before any participant engages in research to ensure they

understand the purpose, risks, and benefits.




What is the role of an Institutional Review Board (IRB)?


✔✔The IRB reviews research proposals to ensure the ethical treatment of human subjects and

compliance with federal regulations.




Why is confidentiality important in human subjects research?


✔✔Confidentiality protects participants’ personal information, ensuring it is not disclosed

without consent, which is crucial for maintaining trust and integrity in research.




1

,What is the main difference between anonymous and confidential data in research?


✔✔Anonymous data means no identifying information is collected, while confidential data

includes identifiers but is protected to prevent unauthorized access.




What are the criteria for exempt research under the Common Rule?


✔✔Research is exempt if it involves minimal risk to participants, such as surveys or

observational studies where the identities of subjects are protected.




When can a waiver of informed consent be granted by the IRB?


✔✔A waiver may be granted when the research poses minimal risk and obtaining consent is

impractical, provided the rights and welfare of participants are not compromised.




What steps should researchers take when working with vulnerable populations?


✔✔Researchers must provide additional protections for vulnerable populations, such as children

or prisoners, to ensure their rights and welfare are safeguarded.




How do federal regulations define minimal risk in research?


✔✔Minimal risk means the likelihood and magnitude of harm or discomfort in the research are

no greater than what is encountered in daily life or routine medical exams.

2

, Why is voluntary participation a key ethical requirement in human subjects research?


✔✔Voluntary participation ensures that individuals choose to participate in research without

coercion, allowing them to withdraw at any time without penalty.




What is the purpose of a continuing review of research by an IRB?


✔✔A continuing review ensures that ongoing research complies with ethical standards and that

no new risks to participants have arisen.




When is research considered non-exempt and thus subject to full IRB review?


✔✔Non-exempt research involves more than minimal risk or includes sensitive information,

requiring full IRB review to evaluate potential ethical concerns.




What are the responsibilities of the principal investigator in human subjects research?


✔✔The principal investigator is responsible for ensuring that the research complies with ethical

guidelines, including obtaining consent and protecting participants' rights.




Why are conflict of interest disclosures important in research involving human subjects?




3

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 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 StellarScores. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for £8.13. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

79373 documents were sold in the last 30 days

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

Start selling
£8.13
  • (0)
  Add to cart