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IRB and IACUC; Questions & Answers 100% Solved

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IRB and IACUC; Questions & Answers 100% Solved D. All the above CORRECT ANSWER-Nuremberg Trials evolved into the Nuremburg Code which laid down the fundamental frame work of ethical medical experimentation. This code included which of the following? A. Requirement that research be voluntary B. That it have benefits to Society C. That it avoid risk and be scientifically qualified D. All the above

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IRB and IACUC; Questions & Answers 100% Solved
D. All the above CORRECT ANSWER-Nuremberg Trials evolved into the Nuremburg Code
which laid down the fundamental frame work of ethical medical experimentation. This code
included which of the following?




A. Requirement that research be voluntary

B. That it have benefits to Society

C. That it avoid risk and be scientifically qualified

D. All the above




C.) The potential risks of the research must not outweigh the potential benefits.
CORRECT ANSWER-The further refinement of the Nuremburg Code that first was adopted in
1964 was called The Declaration of Helsinki. Which of the following statements about the
Declaration are correct?

A.) Research on humans can be conducted by anyone

B.) Research on humans can begin as soon as the P.I. gets funding.

C.) The potential risks of the research must not outweigh the potential benefits.

D.) Human and animal research should be conducted sumultaneously.




A.) IRBs

B.) DHHS Office of Human Research Protections CORRECT ANSWER-The National
Research Act of 1974, a result of the Tuskegee Syphilis Study (1932-1972) established (pick two
of four)

A.) IRBs

, IRB and IACUC; Questions & Answers 100% Solved
B.) DHHS Office of Human Research Protections

C.) Belmont Report

D.) The Colbert Report




3.) A federal wide assurance (FWA) number CORRECT ANSWER-When an entity wishes to
create an IRB to conduct research with human subjects, what do they get to demonstrate that
they have committed to do everything required by DHHS?

1.) A parade

2.) A letter of declaration from their congressman

3.) A federal wide assurance (FWA) number

4.) A state license to experiment on human subjects




C.) Full, expedited & exempt CORRECT ANSWER-Types of IRB review:

A.) Red, yellow, & green

B.) Levels 1, 2 & 3

C.) Full, expedited & exempt

D.) Large, medium & small




C.) the study details, funding source and risk vs. benefit CORRECT ANSWER-Before an IRB
will approve a human research proposal, they will want to know the following:

A.) Names and addresses of human subjects

B.) How much money the study will bring to the institution

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