If you're a mod get a life

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.

Dumb question? (thats me name: ) can a stakeholder be a leader of an organization?

You find a body in a kitchen with undigested eggs and bacon in its stomach. knowing the victim had a set routine they followed most mornings, what would you then check to most narrow in on the time of death? what time the victim’s alarm clock was set to that morning what time the victim goes to work that morning what time the victim usually ate breakfast what time the victim usually took a shower in the morning.