A subject in a clinical research trial experiences a serious, unanticipated adverse drug experience. How should the investigator
proceed, with respect to the IRB, after the discovery of the adverse event occurrence? A. Do not report the adverse drug experience to the IRB since it is a common adverse experience.
B. Report the adverse drug experience to the IRB only if there are several other occurrences.
C. Report the adverse drug experience as part of the continuing review report.
D. Report the adverse drug experience in a timely manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism provided by the IRB
The right covers a number of issues centered on the right of the accused or the defendant to refuse to comment or provide an answer when questioned, either prior to or during legal proceedings in a court of law.
