Maurice Tutor

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Algebra,Applied Sciences,Biology,Calculus,Chemistry,Economics,English,Essay writing,Geography,Geology,Health & Medical,Physics,Science Hide all
Teaching Since: May 2017
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  • MCS,PHD
    Argosy University/ Phoniex University/
    Nov-2005 - Oct-2011

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  • Professor
    Phoniex University
    Oct-2001 - Nov-2016

Category > Management Posted 27 Feb 2018 My Price 5.00

Food andDrug Administration

9.11 Many consumer groups feel that the U.S. Food andDrug Administration (FDA) drug approval process is tooeasy and, as a result, too many drugs are approved that arelater found to be unsafe. On the other hand, a number ofindustry lobbyists have pushed for a more lenient approvalprocess so that pharmaceutical companies can get newdrugs approved more easily and quickly. Consider a nullhypothesis that a new, unapproved drug is unsafe and analternative hypothesis that a new, unapproved drug is safe.a. explain the risks of committing a type I or type II error.b. Which type of error are the consumer groups trying toavoid? explain.c. Which type of error are the industry lobbyists trying toavoid? explain.d. How would it be possible to lower the chances of bothtype I and type II errors?

 


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Maurice Tutor
(5)
Status NEW Posted 27 Feb 2018 08:02 PM My Price 5.00

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