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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.
Answers: 2
Law, 16.07.2019 23:20
The occupational safety and health administration promulgated a rule requiring warehouse employees to wear hardhats when in the vicinity of an operating forklift. the purpose of the hardhats is to protect employees from danger of falling objects. this rule is
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Law, 19.07.2019 04:30
How does an infraction escalate to more serious cases like a misdemeanor and so on? i’ve always wanted to know.
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Law, 25.07.2019 00:10
Science does not rely ideas based on opinions instead of facts because science works to avoid the influence of opinions and beliefs. objective observable proven subjective
Answers: 1
What is the meaning of law?...
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