Question

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.

Answer 1

Question Completion:

Options:

1. Reviewing manuscripts prior to submission for publication.
2. Reviewing subject recruitment materials and strategies.
3. Protecting the rights and welfare of human subjects.
4. Conducting inquiries into scientific misconduct.
5. Assuring that researchers follow all applicable institutional policies and federal regulations related to research with human subjects.

Answer:

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:

Protecting the rights and welfare of human subjects.

Step-by-step explanation:

The IRB monitors biomedical researches. It, especially, protects the rights and welfare of the human subjects that may be used in such researches. This protection is necessary to ensure that the organizations or individuals that are conducting the biomedical research activities do not endanger the life and health of human participants, especially those recruited for the tests.

Answer 2

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 Protecting the rights and welfare of human subjects.

for better understanding we have to explain what Review Board (IRB) is

from the above we can therefore say that the answer 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 Protecting the rights and welfare of human subjects is correct

learn more about Review Board (IRB) from: