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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, 09.07.2019 05:20
How does henry’s statement reflect the idea of social contract? how does the idea of social contract protect people’s natural and individual rights
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Law, 15.07.2019 22:40
How has the sentence for felony murder for minors changed over time?
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The principle of judicial review is traced back to the case of...
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