The was a result of the National Research Act, which created the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. A. Declaration of Helsinki
B. Belmont Report
C. IRB

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.

When was virginia conflict of interest and ethics advisory council created?

"magic" mushrooms have effects similar to those of a. lsd b. pcp c. ketamine d. none of the above