Which of the statements below is true about pharmaceutical or drug packaging? a.) FDA maintains tight control over regulations b.) cost is a major consideration when designing a package c.) advertising and communicating with the consumer is important for both prescription and OTC drugs. d.) shelf life is always shorter than for food so must choose material appropriately.
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Which of the statements below is true about pharmaceutical or drug packaging?
a.) FDA maintains tight control over regulations
b.) cost is a major consideration when designing a package
c.) advertising and communicating with the consumer is important for both prescription and OTC drugs.
d.) shelf life is always shorter than for food so must choose material appropriately.
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- The Food and Drug Administration (FDA) is responsible for: A. Requiring drug manufacturers to provide notice that a new drug is safe. B. Recalling pharmaceuticals only after harm has occurred. C. The approval before a new drug can be marketed. D. The assumption that the manufacturer of drugs would have conducted safety tests before marketing a new drug and protocols have been established.The acronym, USP, referenced on the Data Analysis page refers to the United States Pharmacopeia. Which of the following statements is not true about the USP? a) mission is to improve global health by issuing public standards and related programs to ensure the quality, safety, and benefits of medicines and foods b) generates chemical reference standards and official test methods for medicines and foods to ensure their quality and safety c) is responsible to provide the U.S. with a reliable, affordable, universal mail service d) is a non-profit scientific organization founded in 1820 in Washington D.C.Compounding pharmacies must follow these regulations, except: A) FDA guidelines B) Skilled Nursing Facility guidelines C) USP guidelines D) State Board of Pharmacy guidelines
- Describe the FDA approval process for assessing the safety and efficacy of a newly developed drug. What are advantages and disadvantages of this process?Choose which rule is violated by the following definition. A veterinarian is a doctor specializing in the care of dogs. A) obscure B) too narrow C) circular D) too broadWhich of the following statements are true about the Hatch-Waxman Act? Select one or more: a. The Act benefits the manufacturer of reference drugs by extending the patent. O b. The Act benefits the manufacturer of reference drugs by eliminating reporting requirements for changes in the manufacturing process. O c. The Act benefits the manufacturer of generics drugs by eliminating reporting requirements for changes in the manufacturing process. O d. The Act benefits the manufacturer of generics drugs by eliminating the need for clinical trials.
- Which of the following statements are true? Select one or more: a. All biosimilars are interchangeable products b. A pharmacist may substitute an interchangeable product without the prescriber's permission. O c. All interchangeable products are biosimilars. O d. A pharmacist may substitute a biosimilar product without the prescriber's permission.Which statement is accurate regarding the Dietary Supplement Health and Education Act (DSHEA) of 1994? Select one: a. It mandates that herel product labels contain accurate information. b. It mandates that herbal product labels state that the products are not intended to diagnose, treat, cure, or prevent disease. c. It requires that herbal products undergo the same rigorous testing as drugs do under the FDA.Injection safety, or safe injection practices, is a set of measures taken to perform injections in an optimally safe manner for patients, healthcare personnel, and others. Question options: A) True B) False
- What are the possible lab hazards that may occur during the processing and manufacturing of drugs in industry?Which of the following is FALSE about provisions of the Dietary Supplement Health and Education Act (DSHEA)? O a. Dietary ingredients in supplements must be federally regulated and generally recognized as safe (GRAS) O b. Dietary supplements must be properly and truthfully labeled O c. DSHEA provided a definition of dietary supplement O d. The FDA is responsible for ensuring that a supplement is safe, unadulterated, and check that it has been produced with good manufacturing practicesWhat is Drugbank? https://go.drugbank.com/ A.A compendium of drugs that are commercially available. B.Drug Gene Interaction database C.FBI storage locker for illegal drugs D. A database of pharmaceutical knowledge about drugs.