A group of nurses are discussing subject involvement in a clinical research trial. Which action would the nurses indicate as being required in order to be compliant with an Institutional Review Board (IRB)?
◦ Provide a listing of all subjects' names who are involved in the research study and circulate to hospital departments.
◦ Informed consent is implied once the subject agrees to participate in a research study.
◦ Contact information provided to subjects in case any problems arise.
◦ The nurse tells a subject involved in a clinical research trial that they cannot terminate the agreement.