DO YOU WANNA RP?? THEN DO IT HERE!! :D i did this cus i am bored and i got nothing to do right now.

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.

How would you answer this question. how could you build your practice as an educator for equity, diversity, and inclusion to avoid the oppression of marginalized populations of students?

How can an environmental law affect a business