‏type of advance medical directive does the AMA recommend? Living will or Durable power of attorney ‏I need a definitive answer to this question, please

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 are the four components of a vehicles control system?

Limbic system disorders are possible explanations for criminal behavior under_theries? a. classical b. psychoanalytic c. criminal anthropology .d biocriminiology