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Physics, 22.06.2019 10:50, milkshakegrande101
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, ayoismeisalex
Two carts, one of mass 2m and one of mass m, approach each other with the same speed, v. when the carts collide, they hook together. assume that positive momentum is to the right. which graph best represents the momentum of both carts over time, before and after the collision?
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Cuanto es un tercio de 5.700 please y...
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