Nj mpje evaluation - Study guides, Class notes & Summaries

nj mpje made easy qustions and correct answers Who decides which schedule a drug is in? - ANSWER-The HHS (Secretary of Human Health Services) gives a scientific evaluation to the attorney general and then pretty much decides which schedule the drug should be in. The attorney general can make a drug schedule 1 on the grounds that it can cause "imminent hazard to the general public" without consulting the secretary of HHS How long does a prescriber have to give a hard copy to the pharmacis...

NJ MPJE MADE EASY EXAM | QUESTIONS & ANSWERS (VERIFIED) | LATEST UPDATE | GRADED A+ Who decides which schedule a drug is in? Correct Answer: The HHS (Secretary of Human Health Services) gives a scientific evaluation to the attorney general and then pretty much decides which schedule the drug should be in. The attorney general can make a drug schedule 1 on the grounds that it can cause "imminent hazard to the general public" without consulting the secretary of HHS How long does ...

NJ MPJE Made Easy Questions and Answers 100% Pass Who decides which schedule a drug is in? The HHS (Secretary of Human Health Services) gives a scientific evaluation to the attorney general and then pretty much decides which schedule the drug should be in. The attorney general can make a drug schedule 1 on the grounds that it can cause "imminent hazard to the general public" without consulting the secretary of HHS How long does a prescriber have to give a hard copy to the pharmacis...

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 drugs met the *standards of strength, quality, and purity in USP* -required that the food or drug label *could not be fal...

NJ MPJE Questions and Answers 2023 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 produ...

NJ MPJE 2022-2023; 521 Questions with 100% Correct Answers 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 Pu...

NJ MPJE 2022-2023; 521 Questions with 100% Correct Answers 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 Pu...

NJ MPJE 2022-2023; 521 Questions with 100% Correct Answers 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 Pu...