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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, 03.07.2019 15:10
Why is the supremacy clause considered to be the root of federalism?
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Law, 13.07.2019 16:10
If the light is green as you approach an intersection, you should: a. cover your brakes b. expect it to change soon c. speed up to enter the intersection
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Law, 15.07.2019 23:10
What was a super predator and how did that effect juvenile sentences?
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History, 20.07.2019 22:50
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