Which of the following is most likely reason that a regulated product may go to market?
A. It has not registered for testing and certification.
B. It contains a high percentage of toxic material.
C. It has passed testing and certification standards.
D. It has been shown to be defective and/or dangerous.

Asubject 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