Under the U.S. Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) regulations, what is the Institutional Review Board (IRB) charged with? Sel... Under the U.S. Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) regulations, what is the Institutional Review Board (IRB) charged with? Select all that apply.
Understand the Problem
The question is asking about the responsibilities of an Institutional Review Board (IRB) as defined by U.S. Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) regulations. You need to identify which of the listed activities are indeed part of the IRB's duties.
Answer
The IRB is charged with reviewing recruitment materials, protecting human subjects, and assuring researchers follow policies and regulations.
The Institutional Review Board (IRB) is charged with: Reviewing subject recruitment materials and strategies, protecting the rights and welfare of human subjects, and assuring that researchers follow all applicable institutional policies and federal regulations related to research with human subjects.
Answer for screen readers
The Institutional Review Board (IRB) is charged with: Reviewing subject recruitment materials and strategies, protecting the rights and welfare of human subjects, and assuring that researchers follow all applicable institutional policies and federal regulations related to research with human subjects.
More Information
Institutional Review Boards (IRBs) are critical for upholding ethical standards in research involving human subjects. They ensure studies are conducted ethically and safely.
Tips
A common mistake is thinking IRBs are responsible for investigating scientific misconduct, which is typically handled by other offices.
Sources
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