Federal mpje graded a - Study guides, Class notes & Summaries

VIRGINIA MPJE EXAM 2024| ACTUAL EXAM WITH 100% CORRECT ANSWERS| GRADED A+ Does Virginia or the Federal government decide who has prescribing authority in VA? - correct answer Virginia does. State law controls who can write valid prescriptions What practitioners can write valid Rx for controlled substances in VA? - correct answer Practitioners of medicine (MD) Practitioners of osteopathy (DO) practitioners of dentistry (dentist, DDS, or DMD) practitioners of podiatry (Podiatrist or DPM-"foot...

Utah MPJE-Federal Law Questions and Answers Graded A+ What does CFR relate to? federal regulations What does USC relate to? united states code (laws) What does UAC relate to? Utah administrative code What does UCA relate to? Utah code annotated (law) What are the 4 parts of negligence? duty (obligation by the individual to conform to a specific standard of conduct) breach- violation of that legal obligation by defendant causation- the breach is the actual and proximate cause...

Ohio MPJE Question Bank 2024 Already Graded A A prescription is written for atenolol 50 mg and dated August 15, 2020. The patient brings the prescription in to be filled on March 1, 2021. Can you legally fill the prescription? a) Yes b) No b (> 6 months) Prescription record must be kept for ______ under federal law, and ______ under Ohio law. a) 3 years, 3 years b) 2 years, 2 years c) 2 years, 3 years d) 2 years, 5 years e) none of the above c Records for poisons must be k...

NORTH CAROLINA MPJE EXAM | QUESTIONS & ANSWERS (VERIFIED) | LATEST UPDATE | GRADED A+ Pure Food and Drug Act of 1906 Correct Answer: prohibited the adulteration and misbranding of foods and drugs in interstate commerce Food, Drug, and Cosmetic Act of 1938 Correct Answer: Core of today's drug laws. No new drug can be marketed/sold until proven safe and approved by FDA. Labels must contain adequate directions for use and warnings about their habit-forming properties Durham-Humphre...

Jurisprudence Exam 1 Graded A+ What is the MPJE? Multistate Pharmacy Jurisprudence Examination that combines federal and state specific questions How many attempts are there per jurisdiction for the MPJE? 5 attempts Brainpower Read More What is the waiting period after a failed MPJE attempt? 30 days What are the 4 competencies of the MPJE? 1: Licensure/personnel (22% of exam) 2: Pharmacist practice (33% of exam) 3: Dispensing requirements (24% of exam) 4: Pharmacy operations (21% of...

NEVADA MPJE LATEST UPDATE GRADED A+ Laws vs. Regulations laws - enacted through a federal or state legislative process regulations - (or rules) provide specific details to help implement the law, and are issued by state regulatory agencies (e.g. state board of pharmacy) FDA Drug Approval Process 1) pre-clinical testing (animals) 2) manufacturer files an investigational new drug (INDA) application with the FDA 3) INDA approval --> begin Phase 1 study, Phase 2, then Phase 3 4) f...

Pharmacy Law MPJE Exam: Federal Law Graded A What did the Federal Controlled Substances Act do? Why was it implemented? concerned in the 1960s about legal and illegal drugs being abused They were given the opportunity to design an act/law Created the DEA to promulgate and enforce the law Legislators very Created a closed system between: manufacturer, distributors, prescriber, dispenser, and patient. What did the Pure Food and Drug Act of 1906 do? Prohibited the adulteration and m...

Ohio MPJE Sullivan Exam Set Questions and Answers Graded A+ 1) A prescription is written for atenolol 50 mg and dated August 15, 2017. The patient brings the prescription in to be filled on March 1, 2018. Can you legally fill this prescription? a) Yes b) No b (March 1, 2018 is past 6 months) 2) Prescription records must be kept for ___________________ under federal law, and ____________________ under Ohio law. a) 3 years, 3 years b) 2 years, 2 years c) 2 years, 3 years d) 2 year...

NJ MPJE EXAM | QUESTIONS & ANSWERS (VERIFIED) | LATEST UPDATE | GRADED A+ Neither _____ nor _____ are required by an *ANDA*. Correct Answer: -pre-clinical animal studies -clinical studies *bioequivalence only Prescription drug advertising is regulated by the _____, while OTC drug advertising is regulated by the _____. Correct Answer: -FDA -FTC (Federal Trade Commission) Any false or misleading statements in a drug advertisement could be considered _____. Correct Answer: -misbrand...

PA MPJE 2024 QUESTIONS AND ANSWERS GRADED A+ Generic drug companies can submit what two abbreviated drug applications? ANDA or 505(b)(2) application What is the key difference between an ANDA and 505(b)(2) application? Drugs submitted under ANDA must be bioequivalent and have same route of administration, strength, and formulation Drugs submitted under 505(b)(2) can have different strength or formulation What Act approved in March of 2020 includes OTC monograph reform? The CARES Ac...