To document that the research participant has voluntarily agreed to participate in the study, the research participant must:A. Pass a test of comprehension.B. Meet with the institution's Institutional Review Board (IRB).C. Sign and date the Informed Consent Form.D. All of the above.

Study participant recruitment cannot begin until the IRB has approved the:A. Informed Consent form.B. Protocol.C. Advertisements.D. All of the above.

As part of the consent process, the federal regulations require researchers to: Recommend that potential subjects discuss their decision to participate with family members. Provide potential subjects with information at the appropriate reading comprehension level. Describe penalties that may be imposed for non-participation. Provide a list of the IRB members who reviewed the protocol.

What information should be provided to an IRB for review at the initiation of a study?

Before each participant can participate in the experiment, they need to:Question 12Select one:a.Sign an informed consentb.Receive a full debriefing about what the study is aboutc.Be told why deception is necessaryd.Be given information about how to obtain additional information about the study

An Investigator participating in a clinical trial is responsible for protecting the rights, safety, and welfare of trial participants. Part of this responsibility is:A. Ensuring all subjects are consented appropriately and documented using the IRB approved Informed Consent form.B. Making sure that target enrollment goals are met.C. Enrolling subjects into the study who meet the exclusion criteria.D. Ensuring that the names of all subjects participating in the study are available to the general public.