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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.

Which lists correctly orders nuclear reactions from most radioactive waste generated to least waste generated within a given period of time? o a. radioactive decay, nuclear fission, nuclear fusion o b. radioactive decay, nuclear fusion, nuclear fission o c. nuclear fusion, nuclear fission, radioactive decay o d. nuclear fission, nuclear fusion, radioactive decay

What is the answer to these problems 30 pt