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Q: pharmaceutical primary packaging
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- Describe the FDA approval process for assessing the safety and efficacy of a newly developed drug. What are advantages and disadvantages of this process?what is a designer drug?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.
- How is Medicaid managedVisit the FDA Web site www.fda.gov: Describe the hot topics (featured topics) the FDA is currently handling. From the Menu section at the bottom of the webpage: Provide the total number of recent warnings the FDA issued in the past year. Choose one of the FDA warnings and provide a complete description of why the warning was issued. Provide a full description of one of the recalls the FDA recommended over the past month. If no recalls were issued in the past month, then provide a full description of a recall issued in the past year.what is the Drug Discovery and Development Process.
- What is the definition of a crude drug? Describe the drug's origins.Choose one of the FDA warnings and provide a complete description of why the warning was issued. Provide a full description of one of the recalls the FDA recommended over the past month. If no recalls were issued in the past month, then provide a full description of a recall issued in the past year.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.
- Outline the general steps from initial drug discovery to IND filing. Add as much detail as you need and feel free to use flow charts, graphics, visuals, as long as is made by you alone and not directly copied-pasted from another source. If an IND is cleared to proceed by the US-FDA, what is the single most important goal of a first-in-human (FIH) clinical trial?Can you Justify in 200 WORDS, the importance of pharmaceutical legislation for the country?In the Middle Ages, the Arabs expanded the field of pharmacology?