Compendia Study guides, Class notes & Summaries

MA MPJE Exam with 1200+Questions and Answers RATED A+ 2023|2024 Why does the government regulate medical drugs? Correct answer: protect people from making risky choices and harming themselves Ma state law, how many hours may a pharmacist work? Correct answer: 12 hours per day Allowing people to care for themselves leads to what? Correct answer: market failures What are the 4 kinds of market failures? Correct answer: public goods Externalities Natural monopolies Information asymmet...

(Solution) NJ MPJE Pharmacy Exam Question, EXAMMASTER, PHARMACY EXAM, NJ LAW, MPJE Practice Questions, PreMPJE Practice Questions, NJ MPJE Made Easy, RX LAW WRONG - CARDS, MPJE NJ exam, Pharmacy law review practice exam, Random Pharmacy Law Questions New Jersey Prescription Blanks non-reproducible, non-erasable safety paper bearing that practitioner's license number Approved by the Division of Consumer Affairs in the Department of Law and Public Safety. MD maintain a record of the recei...

How many members are on the Board of Pharamcy - Answer 13 list the members (including how many) of the board of pharmacy - Answer - 8 Registered pharmacists in the state of MA (aka the commonwealth) - 1 licensed pharmacy technician - 1 representative of the public that has experience in health care service delivery, administration or consumer advocacy - 1 physician - 1 nurse - 1 expert in patient safety or quality improvement Of the pharmacists that are on the board of pharmacy in M...

PSB 411 Law Exam 1 Review Chapter 1 Law: a framework through which people in a society resolve their disputes and problems in a way that does not involve force and consistently yields results that are acceptable to most of society Government regulates medicinal drugs very heavily because of the potential risks to users Orphan Drugs: sufficiently safe and effective to be marketed by the number of patients who need them is so small that it is not commercially feasible for manufacturer...

Neither _____ nor _____ are required by an *ANDA*. -pre-clinical animal studies -clinical studies *bioequivalence only Prescription drug advertising is regulated by the _____, while OTC drug advertising is regulated by the _____. -FDA -FTC (Federal Trade Commission) Any false or misleading statements in a drug advertisement could be considered _____. - misbranding Pure Food and Drug Act (1906) description -mandated accurate product labeling and required that the ingredients used in drug...

Neither _____ nor _____ are required by an *ANDA*. - Answer--pre-clinical animal studies -clinical studies *bioequivalence only Prescription drug advertising is regulated by the _____, while OTC drug advertising is regulated by the _____. - Answer--FDA -FTC (Federal Trade Commission) Any false or misleading statements in a drug advertisement could be considered _____. - Answer--misbranding Pure Food and Drug Act (1906) description - Answer--mandated accurate product labeling and requi...

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: -misbranding Pure Food and Drug Act (1906) description Correct Answer: -mandated accurate p...

Pure Food and Drug Act - Answer 1906 - Forbade the manufacture or sale of mislabeled or adulterated food or drugs, it gave the government broad powers to ensure the safety and efficacy of drugs in order to abolish the "patent" drug trade. Still in existence as the FDA. The Food Drug and Comestic Act of 1938 - Answer Established the Food and Drug Administration (FDA). Primarily regulates drug development, manufacturing, and marketing- focus on quality. Only safe and properly labeled dr...

Which of the following brand name products may not be substituted under New York's "negative formulary"? - Phenergan IR tablets, suppositories, solution for injection, oral suspension correct answers A-rated generic product and is NOT -Enteric-coated -Sustained-release (ER, etc.) -Suppository -Injectable suspension Therapeutic equivalents that may be substituted must be... correct answers Bioequivalent and approved ANDA What are some enforcement tools utilized by the FDA? correct an...

En este resumen describí en 30 paginas puntuales el manejo del paciente traumatizado , de esta manera es un libro que pueden leer fácilmente en sus emergencias o en el transporte yendo al trabajo.