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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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Law, 06.07.2019 06:20
Acash payment of $1 given to support a gift promise cannot support a contract. true false
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Law, 07.07.2019 02:10
Cases that arent resloved through plea bargaining or by a jury trial are decided by a judge in a /an? a.indictment b.grand jury c.arraignment d.bench trial
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Law, 08.07.2019 06:10
How has naturalization made an impact or change in society, government, and the political process?
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How does social change happen?...
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