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West Virginia MPJE Latest UPDATED Exam Questions and CORRECT Answers $9.99   Add to cart

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West Virginia MPJE Latest UPDATED Exam Questions and CORRECT Answers

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West Virginia MPJE Latest UPDATED Exam Questions and CORRECT Answers how many public members (non-pharmacists) serve of the BOP? - Correct ANSWER- 2 citizen members (who do not perform any services related to the practice of the pharmacist care) how many pharmacists members serve of the BOP? ...

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  • July 22, 2024
  • 33
  • 2023/2024
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  • West Virginia MPJE
  • West Virginia MPJE
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West Virginia MPJE Latest UPDATED Exam Questions and CORRECT Answers how many public members (non -pharmacists) serve of the BOP? - Correct ANSWER - 2 citizen members (who do not perform any services related to the practice of the pharmacist care) how many pharmacists members serve of the BOP? must they be actively practicing? - Correct ANSWER - -5 licensed pharmacists in WV -no, but must have an active license and be in good standing what is the term of service for BOP members? - Correct ANSWER - after the initial appointment term, the appointment term is 5 years. A member may not serve >2 consecutive terms. A member who has served 2 consecutive full terms may not be reappointed for at least 1 year after completion of his or her 2nd full term. A member may continue to serve until his or her successor has been appointed and qualified when is an IND submitted to the FDA? - Correct ANSWER - after preclinical animal research indicates a relatively safe drug with a potential therapeutic use when is an NDA or BLA submitted to the FDA? - Correct ANSWER - if Phase III trials are submitted successfully what is a sNDA used for? - Correct ANSWER - when a product has a new label, formulation, package, manufacture, or indication what is aNDA used for? - Correct ANSWER - generic drugs what are NADA and ANADA used for? - Correct ANSWER - new animal drug application and abbreviated new animal drug application (generic) t/f? a grandfathered unapproved drug will have an NDC # and will be listed in the FDA's Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) - Correct ANSWER - false, will have NDC #, not in Orange Book _____ attempted to outlaw monopolies that blocked competition by nefarious methods, like price -fixing, deceptive marketing practices, and excluding competition from markets - Correct ANSWER - Sherman Antitrust Act of 1890 _____ means the drug itself is bad (drug quality is not up to standard) - Correct ANSWER - adulteration _____ means the drug label is inaccurate - Correct ANSWER - misbranding what law mandated accurate product labeling and required ingredients to meet standards of strength, quality, and purity in the USP and NF? - Correct ANSWER - Pure Food and Drug Act of 1906 (Wiley Act) which law made a clear distinction between OTC and Rx drugs? - Correct ANSWER - Durham -
Humphrey Amendment of 1951 what are legend drugs? - Correct ANSWER - Rx drugs what law required for the first time that manufacturers prove to the FDA that a drug is both safe and effective for the claims made in the product's labeling, and created the NDA and sNDA? - Correct ANSWER - Kefauver -Harris Amendment of 1962 what law required all Rx and OTC drugs to have a unique NDC number? - Correct ANSWER - Drug Listing Act of 1972 what do the different segments of NDC number mean? - Correct ANSWER - first 4 or 5 numbers are labeler (manufacturer) code second is 3 or 4 numbers identifying strength, dosage, and formulation third is package code identifying package size and type and is 1 or 2 numbers t/f? the poison prevention and packaging act of 1970 deals with Rx drugs and the federal anti -
tampering act of 1982 deals with OTC drugs - Correct ANSWER - true what law made falsely billing Medicare and Medicaid a federal crime? - Correct ANSWER - Federal False Claims Act of 1982 what law established the ANDA and the 505(b)(2) application (paper NDA) for generic drug approval, and established the Orange Book? - Correct ANSWER - Hatch -Waxman Act (Price Competition and Patent Act) of 1984 what law stated that all patients should receive counseling on their medications? - Correct ANSWER - Omnibus Budget Reconciliation Act of 1990 (OBRA 90) how often are pharmacist licenses renewed in WV? What is the due date? - Correct ANSWER - biennial, June 30 what are the CE requirements for WV? - Correct ANSWER - 30 hours per 2 years: 6 hours live, minimum of 3 hours of drug diversion 4 hours immunization if immunizing pharmacist what are the required intern hours for pharmacist licensure in WV? - Correct ANSWER - 1500 hours how long is a WV intern license valid before it expires? - Correct ANSWER - 1 year t/f? the intern hours for a WV license must be completed under the instruction and supervision of a pharmacist - Correct ANSWER - true will the WVBOP accept internship hours completed outside of WV? - Correct ANSWER - yes, need a letter of credit from that state's BOP or from the school where you completed the experience up to 1/3 can be in a foreign country, need letter of credit from the responsible body are criminal background checks required in WV? - Correct ANSWER - as of July 1, 2017, all initial license applications for interns, pharmacists, technicians, and technician trainees require one what are the requirements for registration of pharmacy technicians in WV? - Correct ANSWER - -written app and pay fees -high school grad or GED -tech training program (or one provided by a pharmacy) approved by BOP like PTCB -pass exam approved by BOP -not alcohol or drug abuser -no felony within 10 years -no misdemeanor or felony related to pharmacy -designated as "technician -in-training" prior to meeting requirements can a pharmacist whose license has been denied, revoked, suspended, or restricted for disciplinary purposes in any jurisdiction be eligible to register as a tech? - Correct ANSWER - no what form is submitted by retail pharmacies, hospitals/clinics, practitioners, teaching institutions, or mid -level practitioners to apply for a DEA number? - Correct ANSWER - DEA Form 224 t/f? there are different registration forms for companies involved w/ manufacturing and distributing controlled substances than for individuals and institutions - Correct ANSWER - true what form is submitted by manufacturers, distributors, researchers, analytical laboratories, importers, and exporters to apply for a DEA number? - Correct ANSWER - DEA Form 225

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