This scientific guideline says that ‘words often have multiple or unclear meanings…[They] can mean different things to different people." Therefore, they should be defined explicitly and used consistently.

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.

What does the first amendment’s right to assemble refer to? the right of a group to express unpopular opinions the right of a group to make false claims the right of a group to meet in groups the right of a group to speak in protest

Who is the official leader of the state?