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MPJE Exam with correct Answers (Graded A) $12.49   Add to cart

Exam (elaborations)

MPJE Exam with correct Answers (Graded A)

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  • Michigan MPJE
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  • Michigan MPJE

MPJE Exam with correct Answers

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  • November 1, 2024
  • 22
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • Michigan MPJE
  • Michigan MPJE
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millyphilip
MPJE Exam with correct Answers



what iiis iithe iiorphan iidrug iiact; ii< ii________ iipeople ii- iiAnswers ii-Provides iitax/licensing
iiincentives iifor iimanufacturers iito iidevelop iidrugs/biologicals iifor iitreatment iiof iirare
iicondition/disease iiaffecting ii<200,000 iipeople


NPI iiis iia ii_______________ iiadministrative iisimplification iistandard, ii__ iidigits,
ii________________ iimay iinot iiobtain iia iiNPI iinumber ii- iiAnswers ii-HIPAA
-10
-- iiveterinarians

Voluntary iiaction iitaken iiby iia iicompany iito iiremove iia iidefective iidrug iifrom iimarket. ii
-Class ii1=
--Class ii2=
---Class ii3= ii- iiAnswers ii-Recall
-Situation iiin iiwhich iithere iiis iia iireasonable iiprobability iithat iithe iiuse iiof iior iiexposure iito
iia iiproduct iiwill iicause iiserious iihealth iiconsequences iior iideath
--Use iior iiexposure iimay iicause iitemporary iior iimedically iireversible iiadverse iihealth
iiconsequences, iior iiwhere iiprobability iiof iiadverse iihealth iiconsequences iiis iiremote
---Use iiof iior iiexposure iito iia iiproduct iiis iinot iilikely iito iicause iiadverse iihealth
iiconsequences


Drug iiapproval iiprocess
Steps ii1-3 ii- iiAnswers ii-1. iiPreclinical ii(animal) iitesting
2. iiInvestigational iinew iidrug iiapplication ii(IND) iioutlines iiwhat iisponsor iiof iinew iidrug
iiproposes iifor iihuman iitesting iiin iiclinical iitrials
3. iiPhase ii1 iistudies ii(usually ii20-80 iipeople)

Drug iiapproval iiprocess ii
Steps ii4-6 ii- iiAnswers ii-4. iiPhase ii2 iistudies ii(typically iifew iidozen iito ii300 iipeople)
5. iiphase ii3 iistudies ii(typically iiinvolve iiseveral iihundred iito ii3000 iipeople)
6. iiPre-NDA iiperiod ii(just iibefore iiNDA iiis iisubmitted), iicommon iitime iifor iiFDA iiand iidrug
iisponsors iito iimeet


Drug iiapproval iiprocess
Steps ii7-9 ii- iiAnswers ii-7. iiSubmission iiof iian iiNDA ii(formal iistep iiasking iiFDA iito
iiconsider iia iidrug iifor iimarketing iiapproval)
8. iiAfter iiNDA iiis iireceived, iiFDA iihas ii60 iidays iito iidecide iiwhether iito iifile iiit iiso iiit iican
iibe iireviewed

,9. iiIf iifiled, iian iiFDA iireview iiteam iiis iiassigned iito iievaluate iithe iisponsors iiresearch iion
iithe iidrugs iisafety/effectiveness


Drug iiapproval iiprocess
Steps ii10-12 ii- iiAnswers ii-10. iiFDA iireviews iiinformation iithat iigoes iion iia iidrugs
iiprofessional iilabeling
11. iiFDA iiinspects iithe iifacilities iiwhere iithe iidrug iiwill iibe iimanufactured iias iipart iiof
iiapproval iiprocess
12. iiFDA iireviewers iiwill iiapprove iithe iiapplication iior iiissue iia iicomplete iiresponse iiletter

Drug iicompanies iimust iisubmit iian ii__________________________ iifor iiapproval iito
iimarket iia iigeneric iiproduct ii- iiAnswers ii-Abbreviated iinew iidrug iiapplication ii(ANDA)


To iigain iiFDA iiapproval, iia iigeneric iidrug iimust: ii(6) ii- iiAnswers ii-1. iiContain iisame
iiactive iiingredients iias iiinnovator iidrug
2. iiBe iiidentical iiin iistrength, iidosage iiform, iiand iiroute iiof iiadministration
3. iiHave iithe iisame iiuse iiindications
4. iiBe iibioequivalent
5. iiMeet iithe iisame iibatch iirequirements iifor iiidentity, iistrength, iipurity, iiand iiquality
6. iiBe iimanufactured iiunder iithe iisame iistrict iiFDA iistandards iiof iigood iimanufacturing
iipractice iiregulations


Number iithat iiidentifies iithe iilabeler/vendor, iiproduct, iiand iipackage iisize, iiand iiis
iiassigned iito iieach iidrug iiproduct iilisted iiunder iisection ii510, iifregistration iiof iiproducers
iiof iidrugs iiand iidevices, iiof iithe iifederal iifood, iidrug, iiand iicosmetic iiact ii- iiAnswers ii-
NDC

If iia iiproduct iihas iian iiNDC, iiis iiit iiFDA iiapproved? ii- iiAnswers ii-Does iinot iiguarantee

Three iiways iito iiviolate iithe iiFood iiDrug iiand iiCosmetic iiAct ii(FD&C) ii- iiAnswers ii-1.
iiAdulteration
2. iiMisbranding
3. iiPlacing iiinto iiinterstate iicommerce iian iiunapproved iidrug

Pregnancy iiwarnings: ii(Changing)
Category iiA:
Category iiB: ii- iiAnswers ii-Only iiif iiclearly iineeded ii(Both)

Pregnancy iiwarnings:
Category iiC:
Category iiD:
Category iiX: ii- iiAnswers ii-C: iiOnly iiif iithe iipotential iibenefit iijustifies iithe iipotential iirisk iito
iithe iifetus
D: iiPositive iievidence iiof iidental iirisk iiexists
X: iiMay iicause iifetal iiharm iiwhen iiadministered iito iia iipregnant iiwomen

, The ii___________________ iiinsert iimust iibe iigiven iito iipatient iiwith iieach iidispensing,
iioriginal iiand iirefills ii- iiAnswers ii-Patient iipackage iiinsert


Community iipharmacy iirequired iito iigive iiPP iiwith ii___________________________

Institutions? ii- iiAnswers ii-each iidispensing, iioriginal iiand iirefills

Institution= iiwith iiadministration iiof iifirst iidose iiand iithen iionce iievery ii30 iidays

Consumer iimedication iiinformation ii- iiAnswers ii-Not iirequired iito iibe iigiven iito iipatient.
iiUsually iigiven iiwith iifirst iifill iiif iiit iiis iigiven. iiNot iiregulated iiby iiFDA


Duties iiof iithe iipharmacy iiboard ii- iiAnswers ii-Protection iiof iithe iipublic ii- iihas iiobligation
iito iidiscipline iilicensees iiwho iihave iiadversely iiaffected iithe iipublics iihealth, iisafety, iiand
iiwelfare
-procure iisamples iiand iilimit iior iiprevent iisale iiof iidrugs iiand iidevices iithat iido iinot
iicomply iiwith iithe iilaw


Members iiof iithe iipharmacy iiboard?
___ iitotal ii- iiAnswers ii-11 iitotal
6 iipharmacists
4 iipublic
1 iipharmacy iitechnician

Members iiof iithe iipharmacy iiboard iiare iiappointed iiby ii____________________
-They iihave ii______________ iiterms, iiand iimay iiserve ii__ iiterms iimax ii- iiAnswers ii-the
iigovernor
-4 iiyear iilong, iimax ii2 iiterms ii+ ii1 iipartial iiterm

Disciplinary iisubcommittee ii(DSC) iiof iithe iiboard iicontains ii__________ iimembers ii-
iiAnswers ii-5 iimembers- ii3 iiprofessional iiand ii2 iipublic


DSC: iihow iiis iifinal iidecision iidetermined? ii- iiAnswers ii-majority iivote. iiONE iipublic
iimember iier iihas iito iivote iiwith iithe iimajority, iior iiit iidoes iinot iipass.


DSC iichairperson iiis ii________________________________ ii- iiAnswers ii-a iipublic
iimember iiappointed iiby iithe iichair iiof iithe iifull iiboard


What iiis iithe iiconsumer iiinformation iinotice? ii(CIN)
When iiis iiit iirequired iito iibe iiposted? ii- iiAnswers ii-notice iito iiconsumers iiabout
iiprescription iidrugs
-If iiengaged iiin iithe iibusiness iiof iiselling iidrugs iiat iiretail iiat iieach iicounter iiover iiwith iiRx
iidrugs iiare iidispensed
(*not iirequired iito iibe iiposted iiif iionly iidispenses iidrugs iifor iiinpatient iiuse iiat iia iihealth
iicare iifacility)

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