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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.
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Physics, 22.06.2019 14:30
Will mark as brainliest how does a catapult increase the trajectory of an object? ps. answer as if u were a 5th grader
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Physics, 22.06.2019 15:50
How many neutrons does plutonium -196 with an atomic number of 78.
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Physics, 22.06.2019 19:30
Petroleum contains energy. a. light b. kinetic c. chemical d. mechanical
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Which is closest to the difference between the order of
magnitude for the frequencies of AM radio w...
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