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Law, 03.07.2019 15:10
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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Law, 15.07.2019 20:30
Which general staff member is responsible for ensuring that assigned incident personnel are fed and have communications, medical support, and transportation as needed to meet the operational objective?
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Law, 16.07.2019 14:10
Which of the following is not a potential distraction that could negatively impact your fitness to drive? a. passengers b. technology c. emotions d. traffic lights
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Which of the following crime scene documentation mediums is most beneficial for
avoiding distortion...
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