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Physics, 22.06.2019 10:50
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.
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Physics, 22.06.2019 22:00
Ne way in which elements differ from each other is the structure of the electron cloud in each element's atoms. in an electron cloud, an electron that is farther away from the nucleus has
Answers: 1
A bike travels at a constant speed of 4.0 m/s for 5.0s. How far does it go?...
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