Miscellaneous questions Flashcards

1
Q

What 3 ethical principles are described in the belmont report?

A
  • Respect for persons
  • Beneficence
  • Justice
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2
Q

To what 3 areas do the rules established in the Belmont report apply?

A
  • Informed consent
  • Assessment of risks and benefits
  • Selection of subjects
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3
Q

What are the 10 principles established with the Nuremberg Code?

A
  1. Voluntary consent
  2. Yield results for the good of society
  3. Design based on animal experiments
  4. Avoid unnecessary suffering and injury
  5. No experiment conducted if death/disabling injury will occur
  6. Benefits outweigh risks
  7. Proper facilities / preparation of site
  8. Qualified persons performing study
  9. Subject can withdraw at any time
  10. Investigator can terminate study at any time
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4
Q

What document (Nuremberg, Belmont, Helsinki) established the need for a legally authorized representative?

A

Declaration of Helsinki.

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5
Q

To whom was the Declaration of Helsinki primarily addressed?

A

Physicians.

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6
Q

What is considered significant equity interest?

A

If the PI gets interest/stock options or any other financial and equity interest during the time of the study and 1 year following completion of the study.
For a publicly traded company, this means more than $50k to PI, spouse or children.

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7
Q

What is considered a significant payment to an investigator in a covered clinical trial? What is considered a covered clinical trial?

A

Payments to the investigator that have a monetary value over $25k (excluding research related payments) during trial or up two 1 year after completion. A covered clinical trial is any submitted in a marketing application for the FDA proving the effectiveness of the drug/device or significantly contributes to product safety.

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8
Q

What is FDA Form 482?

A

“Notice of Inspection” Form. From FDA to sponsor letting them know that they are coming to inspect (not necessarily bad).

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9
Q

What is FDA Form 483?

A

“Inspectional Observations” Form. This is the result of the FDA audit telling the sponsor what they need to fix (Not good).

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