Answers: 2
Law, 16.07.2019 18:20
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
Answers: 1
Law, 23.07.2019 06:10
Geographic expeditions, inc. (geoex), which guided climbs up mount kilimanjaro, required climbers to sign a release to participate in an expedition. the form required any disputes to be submitted to arbitration in san francisco and limited damages to the cost of the trip. geoex told climbers that the terms were nonnegotiable and that other travel firms imposed the same terms. jason lhotka died on a geoex climb. his mother filed a suit against geoex. geoex sought arbitration. was the arbitration clause unconscionable? why or why not?
Answers: 3
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