Pharmaceutical Analysis Quiz
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Questions and Answers

What is the main purpose of Quality Control (QC) in drug production?

  • To perform routine RM and PM analysis on the finished product
  • To conduct stability studies on intermediate stage analysis (ISA)
  • To guarantee that the product is free of impurities and contains the stated amount of active ingredients (correct)
  • To ensure that the product meets minimum standards for strength, quality, purity, packaging, and labeling

    • What are the implications of poor quality drugs, as mentioned in the text?

  • Reduced availability, lack of reliable drug quality assurance systems, and wasted resources
  • Calibration and preventive maintenance, intermediate stage analysis, and finished product analysis
  • Treatment failure, adverse effects, increased morbidity, mortality, and development of drug resistance (correct)
  • Increased production costs, lack of stability studies, and routine RM and PM analysis

    • What is the reality of drug quality in many low-income countries?

  • Calibration and preventive maintenance
  • Availability of substandard and counterfeit drugs in disturbing proportion (correct)
  • Lack of reliable drug quality assurance systems in many developing countries
  • Routine RM and PM analysis

    • What does Drug quality assurance systems in many developing countries lack, according to the text?

    <p>Reliable drug quality assurance systems</p> Signup and view all the answers

    What does Quality Control (QC) guarantee about the product?

    <p>Physically and Chemically Stable</p> Signup and view all the answers

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